H00427  Relapsing fever

       H00042  Glioma
       H01692  Subependymal giant cell astrocytoma
       H02942  Melanoma-astrocytoma syndrome
       H01667  Medulloblastoma
       H01007  Choroid plexus papilloma

       H01556  Meningioma

       H00043  Neuroblastoma

       H00003  Acute myeloid leukemia
       H02542  Acute promyelocytic leukemia

           H01510  Malignant paraganglioma

       H01558  Parathyroid carcinoma

         H01471  Lymphangioma
         H01735  Lymphangiomatosis
         H01482  Infantile hemangioma
         H01875  Infantile hepatic hemangioma

         H01640  Uterine leiomyoma

         H00804  Multiple cutaneous and uterine leiomyomata

         H02922  Pleomorphic salivary gland adenoma

         H02538  Pheochromocytoma/paraganglioma syndrome
         H01025  Familial adenomatous polyposis
         H00539  PTEN hamartoma tumor syndrome
         H01023  Juvenile polyposis syndrome
         H01024  Hereditary mixed polyposis syndrome
         H02795  Sessile serrated polyposis cancer syndrome
         H02869  Familial hepatic adenomas

           H02756  Congenital juvenile recurrent respiratory papillomatosis

           H02874  Congenital melanocytic nevus syndrome
           H02875  Neurocutaneous melanosis

           H02921  Seborrheic keratosis

           H00827  Brooke-Spiegler syndrome
           H00828  Familial cylindromatosis
           H00829  Multiple familial trichoepithelioma
           H00947  Pilomatricoma
           H02954  Steatocystoma multiplex

           H01910  Infantile myofibromatosis

         H01691  Renal angiomyolipoma

         H01149  Ring dermoid of cornea

         H01102  Pituitary adenomas

       H00247  Multiple endocrine neoplasia syndrome
       H03073  Paraganglioma and gastric stromal sarcoma

       H01134  Rhabdoid predisposition syndrome
       H02624  Tumor predisposition syndrome

     2F90  Neoplasms of unknown behaviour of oral cavity or digestive organs
     2F91  Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs
     2F92  Neoplasms of unknown behaviour of skin
     2F93  Neoplasms of unknown behaviour of retroperitoneum
     2F94  Neoplasms of unknown behaviour of peritoneum
     2F95  Neoplasms of unknown behaviour of breast
     2F96  Neoplasms of unknown behaviour of female genital organs
     2F97  Neoplasms of unknown behaviour of male genital organs
     2F98  Neoplasms of unknown behaviour of urinary organs
     2F99  Neoplasms of unknown behaviour of eye or ocular adnexa
     2F9A  Neoplasms of unknown behaviour of endocrine glands
     2F9B  Neoplasms of unknown behaviour of bone or articular cartilage
     2F9C  Neoplasms of unknown behaviour of connective or other soft tissue
     2F9Y  Neoplasms of unknown behaviour of other specified site
     2F9Z  Neoplasms of unknown behaviour of unspecified site

       H01132  Aplastic anemia
       H00238  Fanconi anemia
       H00439  Shwachman-Diamond syndrome
       H00507  Dyskeratosis congenita
       H00788  Hoyeraal-Hreidarsson syndrome
       H00921  Revesz syndrome
       H02524  Ataxia-pancytopenia syndrome
       H02529  Bone marrow failure syndrome
       H02569  Pulmonary fibrosis and/or bone marrow failure, telomere-related
       H02608  Autoinflammatory-pancytopenia syndrome

       H00978  Thrombocytopenia (THC)
       H00227  Congenital amegakaryocytic thrombocytopenia
       H00233  MYH9-related disease
       H00578  Epstein syndrome
       H00867  Radioulnar synostosis with amegakaryocytic thrombocytopenia
       H01740  Macrothrombocytopenia
       H01847  Thrombocytopenia-absent radius syndrome
       H02052  Sebastian syndrome
       H02053  Fechtner syndrome
       H01240  Immune thrombocytopenia
       H02979  Fetomaternal alloimmune thrombocytopenia
       H00225  Thrombotic thrombocytopenic purpura

       H02749  Bleeding disorder vascular-type

       H01761  Immunoglobulin G4-related disease
       H01502  Sjogren syndrome
       H01710  Mixed connective tissue disease
       H01693  Eosinophilic fasciitis
       H01133  Reynolds syndrome
       H01232  Syndromic multisystem autoimmune disease
       H02540  Infantile-onset multisystem autoimmune disease
       H03012  Autoinflammation and autoimmunity, systemic, with immune dysregulation

         H01598  Addison disease
         H00177  Neonatal adrenoleukodystrophy
         H00256  Familial glucocorticoid deficiency
         H00257  Achalasia Addisonianism Alacrima syndrome
         H02314  Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete
         H02316  Adrenal insufficiency, NR5A1 related
         H02319  IMAGE syndrome

         H02019  Familial male-limited precocious puberty
         H02027  Male hypogonadism

         H02736  Neurodegeneration and seizures due to copper transport defect
         H00210  Wilson disease
         H00209  Menkes syndrome
         H03053  Huppke-Brendel syndrome
         H02938  L-ferritin deficiency
         H00833  Neurodegeneration with brain iron accumulation
         H02207  Kufor-Rakeb syndrome
         H02208  Pantothenate kinase-associated neurodegeneration
         H02209  HARP syndrome
         H02970  Neurodevelopmental disorder with epilepsy and hemochromatosis
         H00211  Hemochromatosis
         H00212  Acrodermatitis enteropathica
         H02550  Birk-Landau-Perez syndrome
         H00213  Hypophosphatasia
         H01113  Acid phosphatase deficiency
         H02138  Hereditary hypophophatemic rickets with hypercalciuria
         H00240  Gitelman syndrome
         H01210  Hypomagnesemia
         H00245  Calcium sensing receptor (CASR) related disease
         H01371  Hypercalcemia infantile
         H03106  Autosomal dominant hypocalcemia
         H03111  Leukoencephalopathy with ataxia
         H01938  Hypermanganesemia with dystonia
         H03105  Hyposulfatemia with skeletal dysplasia

       H01453  Obsessive-Compulsive and Related Disorder

     6D10  Personality disorder
     6D11  Prominent personality traits or patterns

     6E60  Secondary neurodevelopmental syndrome
     6E61  Secondary psychotic syndrome
     6E62  Secondary mood syndrome
     6E63  Secondary anxiety syndrome
     6E64  Secondary obsessive-compulsive or related syndrome
     6E65  Secondary dissociative syndrome
     6E66  Secondary impulse control syndrome
     6E67  Secondary neurocognitive syndrome
     6E68  Secondary personality change
     6E69  Secondary catatonia syndrome
     6E6Y  Other specified secondary mental or behavioural syndrome
     6E6Z  Secondary mental or behavioural syndrome, unspecified

       H01727  Primary alveolar hypoventilation syndrome
       H01729  Premature ventricular complexes
       H01715  Obesity hypoventilation syndrome
       H00916  Congenital central hypoventilation syndrome

     7B00  Disorders of arousal from non-REM sleep
     7B01  Parasomnias related to REM sleep
     7B02  Other parasomnias
     7B0Y  Other specified parasomnia disorders
     7B0Z  Parasomnia disorders, unspecified

       H00577  Symptomatic generalized epilepsies
       H00808  Idiopathic generalized epilepsies
       H02889  X-linked epilepsy-2 with or without impaired intellectual development and dysmorphic features
       H01247  Pyridoxine-dependent epilepsy
       H01819  Early myoclonic encephalopathy
       H02250  Early-onset vitamin B6-dependent epilepsy
       H02696  Early-onset epilepsy
       H00806  Benign familial neonatal seizure
       H03048  Familial infantile convulsions with paroxysmal choreoathetosis
       H01818  Dravet syndrome
       H01815  Malignant migrating partial seizures in infancy
       H01775  PCDH19-related epilepsy syndrome
       H02212  Familial infantile myoclonic epilepsy
       H02215  Childhood absence epilepsy
       H01823  Myoclonic-astatic epilepsy
       H01822  Epilepsy with myoclonic absence
       H01258  Generalized epilepsy and paroxysmal dyskinesia
       H02361  Myoclonic-atonic epilepsy
       H02564  Generalized epilepsy with febrile seizures plus
       H02939  Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp
       H02217  Juvenile myoclonic epilepsy
       H02216  Juvenile absence epilepsy
       H02213  Familial adult myoclonic epilepsy
       H00809  Familial epilepsy temporal lobe (ETL)
       H00810  Progressive myoclonic epilepsy
       H01212  Familial encephalopathy with neuroserpin inclusion bodies
       H01994  Myoclonic epilepsy of Lafora
       H01995  Unverricht-Lundborg disease
       H00807  Nocturnal frontal lobe epilepsy
       H00836  GLUT1 deficiency syndrome
       H02214  Familial focal epilepsy with variable foci

         H00821  Age-related macular degeneration
         H01480  Idiopathic macular hole
         H01010  Occult macular dystrophy
         H01651  Macular edema
         H03030  Early-onset macular degeneration

     9D90  Vision impairment including blindness
     9D92  Specific vision dysfunctions
     9D93  Complex vision-related dysfunctions
     9D94  Impairment of presenting visual acuity
     9D95  Impairment of best corrected visual acuity
     9D96  Impairment of uncorrected visual acuity
     9D9Y  Other specified vision impairment
     9D9Z  Vision impairment, unspecified

     CB60  Tracheostomy malfunction
     CB61  Chronic pulmonary insufficiency following surgery
     CB62  Postprocedural subglottic stenosis
     CB63  Postprocedural stenosis of the trachea
     CB64  Transfusion related acute lung injury

         H00795  Seborrhea-like dermatitis with psoriasiform element
         H01652  Seborrheic dermatitis

             H01445  Acne vulgaris

       H00448  Familial osteochondritis dissecans
       H01526  Legg-Calve-Perthes Disease
       H01529  Avascular necrosis of femoral head
       H01758  Relapsing polychondritis

       H02193  Intrahepatic cholestasis of pregnancy

     JA80  Maternal care related to multiple gestation
     JA81  Maternal care related to complications specific to multiple gestation
     JA82  Maternal care for malpresentation of fetus
     JA83  Maternal care for disproportion
     JA84  Maternal care for abnormality of pelvic organs
     JA85  Maternal care for fetal abnormality or damage
     JA86  Maternal care for other fetal problems
     JA87  Maternal care related to polyhydramnios
     JA88  Maternal care related to certain specified disorders of amniotic fluid or membranes
     JA89  Maternal care related to premature rupture of membranes
     JA8A  Maternal care related to placental disorders
     JA8B  Maternal care related to placenta praevia or low lying placenta
     JA8C  Maternal care related to premature separation of placenta
     JA8D  Maternal care related to false labour
     JA8E  Maternal care related to prolonged pregnancy
     JA8Y  Maternal care related to other specified fetus, amniotic cavity or possible delivery problems
     JA8Z  Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems

     KA00  Fetus or newborn affected by maternal conditions that may be unrelated to present pregnancy
     KA01  Fetus or newborn affected by maternal complications of pregnancy
     KA02  Fetus or newborn affected by complications of placenta
     KA03  Fetus or newborn affected by complications of umbilical cord
     KA04  Fetus or newborn affected by other abnormalities of membranes
     KA05  Fetus or newborn affected by certain complications of labour or delivery
     KA06  Fetus or newborn affected by noxious influences transmitted via placenta or breast milk
     KA07  Neonatal dermatoses due to maternal antibodies
     KA0Z  Fetus or newborn affected by unspecified maternal factors or by complications of pregnancy, labour or delivery

     KA20  Disorders of newborn related to slow fetal growth or fetal malnutrition
     KA21  Disorders of newborn related to short gestation or low birth weight, not elsewhere classified
     KA22  Disorders of newborn related to long gestation or high birth weight
     KA2Y  Other specified disorders of newborn related to length of gestation or fetal growth
     KA2Z  Disorders of newborn related to length of gestation or fetal growth, unspecified

       H01211  MECP2-related severe neonatal encephalopathy

     KB20  Intrauterine hypoxia
     KB21  Birth asphyxia
     KB22  Metabolic acidaemia in newborn
     KB23  Respiratory distress of newborn
     KB24  Congenital pneumonia
     KB25  Neonatal tracheitis
     KB26  Neonatal aspiration syndromes
     KB27  Pulmonary air leak or related conditions originating in the perinatal period
     KB28  Pulmonary haemorrhage originating in the perinatal period
     KB29  Chronic respiratory disease originating in the perinatal period
     KB2A  Apnoea of newborn
     KB2B  Primary atelectasis of newborn
     KB2C  Cyanotic attacks of newborn
     KB2D  Respiratory failure of newborn
     KB2E  Respiratory arrest of newborn
     KB2F  Congenital lung or lobar atelectasis
     KB2G  Tracheal haemorrhage of newborn due to airway trauma
     KB2H  Acquired vocal cord paralysis in newborn
     KB2J  Airway obstruction in the neonate due to airway abnormality
     KB2K  Pulmonary cysts in newborn
     KB2Y  Other specified respiratory disorders specific to the perinatal or neonatal period
     KB2Z  Respiratory disorders specific to the perinatal or neonatal period, unspecified

       H00530  Joubert syndrome and related disorders
       H00897  Pontocerebellar hypoplasia
       H01001  COACH syndrome
       H01811  Arima syndrome
       H02272  CAPOS syndrome
       H02431  Cerebellar hypoplasia, epilepsy, and global developmental delay
       H02464  Poretti-Boltshauser syndrome
       H02833  Brain malformation renal syndrome
       H03016  Valence-Farazi cerebellar ataxia syndrome
       H00268  Lissencephaly
       H00792  Warburg micro syndrome
       H02117  Neu-Laxova syndrome
       H00616  Bowen-Conradi syndrome
       H00840  Pseudo-TORCH syndrome
       H00990  Microcephaly, Amish type
       H00991  Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II)
       H00993  Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I)
       H01872  Microcephaly-capillary malformation syndrome
       H01876  Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
       H01921  MICPCH syndrome
       H02132  Microcephaly syndrome
       H02282  Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
       H02461  Neurodevelopmental disorder with microcephaly
       H02492  Microcephaly, growth restriction, and increased sister chromatid exchange
       H02668  Heyn-Sproul-Jackson syndrome
       H02707  Khan-Khan-Katsanis syndrome
       H02708  Baralle-Macken syndrome
       H02709  Neurodevelopmental disorder with aminoacyl-tRNA synthetase defect
       H02726  Kaya-Barakat-Masson syndrome
       H02808  Childhood-onset neurodegeneration with progressive microcephaly
       H02881  Jawad syndrome
       H03033  Progressive microcephaly with simplified gyral pattern and cerebellar hypoplasia
       H00544  Septo-optic dysplasia
       H00816  Agenesis of the corpus callosum with peripheral neuropathy
       H01034  L1 syndrome
       H01035  Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia
       H01776  Aicardi syndrome
       H01789  You-Hoover-Fong syndrome
       H01919  Proud syndrome
       H01937  Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly
       H02366  Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
       H02396  Corpus callosum agenesis with facial anomalies and cerebellar ataxia
       H02487  Diencephalic-mesencephalic junction dysplasia syndrome
       H02519  Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
       H02606  Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
       H02645  Cerebellar atrophy with seizures and variable developmental delay
       H02652  Macrocephaly, acquired, with impaired intellectual development
       H02653  Faundes-Banka syndrome
       H02680  Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities
       H02695  Fibrosis, neurodegeneration, and cerebral angiomatosis
       H02723  Macrocephaly/autism syndrome
       H02745  Neuromuscular oculoauditory syndrome
       H02776  Ventriculomegaly and arthrogryposis
       H02785  Band heterotopia
       H02825  Megalencephaly-polydactyly syndrome
       H02839  Infantile-onset neurodegeneration with optic atrophy and brain abnormalities
       H02840  Morimoto-Ryu-Malicdan neuromuscular syndrome
       H02925  Early-childhood-onset neurodegeneration with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy
       H02951  Ventriculomegaly with cystic kidney disease
       H02966  Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism
       H03007  Nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus
       H03057  CEBALID syndrome

       H00520  Type II collagenopathies
       H00505  FGFR3-related short limb skeletal dysplasia
       H01749  Achondroplasia
       H02069  SADDAN
       H02068  Hypochondroplasia
       H01750  Thanatophoric dysplasia
       H00515  Atelosteogenesis type II
       H02063  Diastrophic dysplasia
       H00207  Rhizomelic chondrodysplasia punctata
       H00447  HEM skeletal dysplasia
       H00496  Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD)
       H01194  X-linked chondrodysplasia punctata
       H00436  Osteopetrosis
       H00452  Buschke-Ollendorff syndrome
       H00434  Camurati-Engelmann disease
       H00444  Osteopathia striata with cranial sclerosis
       H00450  Worth type autosomal dominant osteosclerosis
       H00486  Sclerosteosis
       H00490  Diaphyseal dysplasia with anemia
       H00491  Craniometaphyseal dysplasia
       H00508  Blomstrand syndrome
       H00613  Infantile cortical hyperostosis
       H00968  Raine syndrome
       H01832  Lenz-Majewski syndrome
       H02631  Melorheostosis
       H02735  Diaphyseal medullary stenosis with malignant fibrous histiocytoma
       H03080  Craniometadiaphyseal osteosclerosis with hip dysplasia
       H00122  Multiple exostoses
       H00493  Heparan sulfate proteoglycan gene defects
       H00497  Cherubism
       H02127  Yunis-Varon syndrome
       H00443  Osteoglophonic dysplasia
       H00498  Gnathodiaphyseal dysplasia
       H00521  Cleidocranial dysplasia
       H01018  Metachondromatosis
       H02558  Craniotubular dysplasia, Ikegawa type
       H00445  Osteoarthritis with mild chondrodysplasia
       H00474  Schneckenbecken dysplasia
       H00483  Angel shaped phalangoepiphyseal dysplasia
       H00499  Spondylocarpotarsal synostosis syndrome
       H00519  Spondyloepiphyseal dysplasia congenita
       H00757  Dyggve-Melchior-Clausen disease
       H00758  Progressive pseudorheumatoid dysplasia
       H00760  Spondyloepiphyseal dysplasia tarda
       H00761  SEMD, Pakistani type
       H00765  Spondyloepiphyseal dysplasia, Kimberley type
       H00767  SEMD, Matrilin type
       H00777  SEMD, short limb-hand type
       H00863  Spondylo-megaepiphyseal-metaphyseal dysplasia
       H01494  SEMD with joint laxity type
       H01575  Roifman syndrome
       H01576  Spondyloenchondrodysplasia with immune dysregulation (SPENCDI)
       H01967  Anauxetic dysplasia
       H02070  Kniest dysplasia
       H02071  Czech dysplasia
       H02079  Oto-spondylo-megaepiphyseal dysplasia
       H02080  Fibrochondrogenesis
       H02155  Dyssegmental dysplasia
       H02183  Parastremmatic dwarfism
       H02184  Metatropic dysplasia
       H02186  Spondyloepiphyseal dysplasia, Maroteaux type
       H02187  Spondyloepimetaphyseal dysplasia
       H02462  Spondyloepiphyseal dysplasia
       H02497  Smith-McCort dysplasia
       H01821  Spondylometaphyseal dysplasia with cone-rod dystrophy
       H01825  Spondylometaphyseal dysplasia, Sedaghatian type
       H01830  Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
       H02185  Spondylometaphyseal dysplasia
       H02732  Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly
       H00678  Achondrogenesis type IA
       H02065  Achondrogenesis type IB
       H02066  Achondrogenesis type II
       H00522  Brachyolmia
       H01828  Opsismodysplasia
       H01844  Diaphanospondylodysostosis
       H00495  Eiken dysplasia
       H00477  Pseudoachondroplasia
       H00476  Multiple epiphyseal dysplasia
       H02436  Al-Gazali syndrome
       H03078  Al-Gazali-Bakalinova syndrome
       H02871  Lowry-Wood syndrome
       H00479  Metaphyseal dysplasias
       H00518  Metaphyseal dysplasia without hypotrichosis
       H02823  Osteosclerotic metaphyseal dysplasia
       H00675  Acrocapitofemoral dysplasia
       H00900  Geleophysic dysplasia
       H02062  Familial digital arthropathy-brachydactyly
       H02228  Acromicric dysplasia
       H02229  Terminal osseous dysplasia
       H00466  Grebe dysplasia
       H00468  Acromesomelic dysplasia, Demirhan type
       H00470  Acromesomelic dysplasia, Maroteaux type
       H02543  Acromesomelic dysplasia
       H02786  ENDOVE syndrome
       H00485  Robinow syndrome
       H00492  SHOX-related short stature
       H02154  Omodysplasia
       H02743  KINSSHIP syndrome
       H03082  Short stature, Dauber-Argente type
       H02157  Short-rib thoracic dysplasia
       H00511  Short rib-polydactyly syndrome
       H00751  Asphyxiating thoracic dystrophy
       H00462  Stuve-Wiedemann syndrome
       H02629  Bent bone dysplasia syndrome
       H02873  Kyphomelic dysplasia
       H00509  3M syndrome
       H00619  Kenny-Caffey syndrome
       H00622  Hypoparathyroidism-retardation-dysmorphism syndrome
       H00992  Seckel syndrome
       H02223  Osteocraniostenosis
       H03024  Saul-Wilson syndrome
       H00494  Desbuquois syndrome
       H01498  Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
       H02048  Larsen syndrome
       H02064  Atelosteogenesis type I and III
       H02067  Boomerang dysplasia
       H00458  Syndromic craniosynostoses
       H01756  Pfeiffer syndrome
       H01754  Crouzon syndrome
       H01755  Apert syndrome
       H01008  C syndrome
       H01753  Antley-Bixler syndrome
       H01888  Carpenter syndrome
       H01988  Jackson-Weiss syndrome
       H01989  Beare-Stevenson syndrome
       H01990  Muenke syndrome
       H01991  Saethre-Chotzen syndrome
       H01992  Craniofrontonasal syndrome
       H01993  Baller-Gerold syndrome
       H02047  Bohring-Opitz syndrome
       H02254  Craniosynostosis and dental anomalies
       H02637  Brachycephaly, trichomegaly, and developmental delay
       H02766  Radiohumeral fusions with other skeletal and craniofacial anomalies
       H02853  Teebi hypertelorism syndrome
       H02932  Scaphocephaly, maxillary retrusion, and impaired intellectual development
       H02949  Robinow-Sorauf syndrome
       H03103  Craniosynostosis-scoliosis syndrome
       H00517  Spondylocostal dysostosis
       H01843  Cerebrocostomandibular syndrome
       H00464  Nail-patella syndrome
       H00461  Ischiocoxopodopatellar syndrome
       H01889  Meier-Gorlin syndrome
       H00506  Osteogenesis imperfecta
       H00451  Osteoporosis-pseudoglioma syndrome
       H00514  Bruck syndrome
       H01496  Spondyloocular syndrome
       H01571  Singleton-Merten syndrome
       H01572  Cole-Carpenter syndrome
       H02395  Calvarial doughnut lesions with bone fragility
       H00969  Skeletal defects, genital hypoplasia, and mental retardation
       H02233  Alazami syndrome
       H02280  Complex lethal osteochondrodysplasia
       H02300  Steel syndrome
       H02306  Chondrodysplasia with joint dislocations, GPAPP type
       H02349  Odontochondrodysplasia
       H02415  Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
       H02551  Skeletal dysplasia with joint laxity and advanced bone age
       H02742  Congenital neuromuscular disorder with dysmorphic facies
       H02801  Osteochondrodysplasia, brachydactyly, and overlapping malformed digits

       H00979  Sacral defect with anterior meningocele
       H02129  Prune belly syndrome
       H01195  VACTERL/VATER association
       H00261  Meckel syndrome
       H01738  Noonan syndrome
       H00610  Treacher Collins syndrome
       H01838  Mandibulofacial dysostosis with microcephaly
       H02126  Mandibulofacial dysostosis with alopecia
       H02211  Acrodysostosis
       H02673  Craniofacial microsomia
       H00433  Holt-Oram syndrome
       H00453  Branchio-oto-renal syndrome
       H00460  Hand-foot-genital syndrome
       H00463  Currarino syndrome
       H00500  Keutel syndrome
       H00502  Pallister-Hall syndrome
       H00504  Rubinstein-Taybi syndrome
       H00510  Feingold syndrome
       H00523  Noonan syndrome and related disorders
       H00555  Char syndrome
       H00556  CHARGE syndrome
       H00569  Aarskog-Scott syndrome
       H00570  Kabuki syndrome
       H00572  Roberts-SC phocomelia syndrome
       H00573  Townes-Brocks syndrome
       H00574  Coffin-Lowry syndrome
       H00583  Opitz-GBBB syndrome
       H00611  Popliteal pterygium syndrome (PPS)
       H00631  Cornelia de Lange syndrome
       H00634  Duane-radial ray syndrome
       H00637  Ulnar-mammary syndrome
       H00685  Bifid nose with or without anorectal and renal anomalies
       H00686  Manitoba oculotrichoanal syndrome
       H00709  Birk Barel mental retardation syndrome (BBMRS)
       H00711  Russell-Silver syndrome
       H00753  Urofacial syndrome
       H00756  Pitt-Hopkins syndrome
       H00797  Martsolf syndrome
       H00817  Branchiooculofacial syndrome
       H00868  Stapes ankylosis with broad thumb and toes
       H00886  Donnai-Barrow syndrome
       H00889  Lujan-Fryns syndrome
       H00894  FG syndrome
       H00907  Kleefstra syndrome
       H00908  Mowat-Wilson syndrome
       H00914  Warsaw breakage syndrome
       H00926  Growth retardation, developmental delay, coarse facies, and early death
       H00934  Caudal duplication anomaly
       H00936  Goldberg-Shprintzen megacolon syndrome
       H00943  TARP syndrome
       H00965  RAPADILINO syndrome
       H00972  Endocrine-cerebro-osteodysplasia syndrome
       H00987  Fetal akinesia deformation sequence
       H00997  CATSHL syndrome
       H01026  Renal coloboma syndrome
       H01030  Congenital arthrogryposis with anterior horn cell disease
       H01156  STAR syndrome
       H01220  Congenital cataracts, facial dysmorphism, and neuropathy
       H01265  Hydrolethalus syndrome
       H01289  Mulibrey nanism
       H01292  Nance-Horan syndrome
       H01370  SHORT syndrome
       H01393  Van Maldergem syndrome
       H01402  Nicolaides-Baraitser syndrome
       H01413  Adams-Oliver syndrome
       H01568  3C syndrome
       H01569  CHOPS syndrome
       H01573  Zimmermann-Laband syndrome
       H01745  Cardiofaciocutaneous syndrome
       H01747  Costello syndrome
       H01793  Young-Simpson syndrome
       H01794  Genitopatellar syndrome
       H01795  Blepharophimosis-mental retardation syndrome
       H01797  Webb-Dattani syndrome
       H01814  Stromme syndrome
       H01839  Burn-McKeown syndrome
       H01840  Moebius syndrome
       H01845  Catel-Manzke syndrome
       H01869  Megacystis microcolon intestinal hypoperistalsis syndrome
       H01878  Al-Raqad syndrome
       H01879  Wiedemann-Steiner syndrome
       H01887  3MC syndrome
       H01908  Carey-Fineman-Ziter syndrome
       H01917  CK syndrome
       H01923  Microcephaly, short stature, and impaired glucose metabolism
       H01927  Van der Woude syndrome
       H01930  Au-Kline syndrome
       H01932  Ablepharon-macrostomia syndrome
       H01984  Leopard syndrome
       H02023  Baraitser-Winter syndrome
       H02046  OFC syndrome
       H02072  Stickler syndrome
       H02074  Knobloch syndrome
       H02082  Floating-Harbor syndrome
       H02087  Vertebral, cardiac, renal, and limb defects syndrome
       H02102  Myhre syndrome
       H02180  McKusick-Kaufman syndrome
       H02190  CBL syndrome
       H02191  Noonan-like syndrome with loose anagen hair
       H02198  Pancreatic agenesis and congenital heart disease
       H02232  CAGSSS syndrome
       H02248  MEND syndrome
       H02249  Primrose syndrome
       H02253  Beaulieu-Boycott-Innes syndrome
       H02255  FDLAB syndrome
       H02260  Chondrodysplasia Chassaing-Lacombe type
       H02271  Cerebellofaciodental syndrome
       H02274  Cerebellar atrophy, visual impairment, and psychomotor retardation
       H02283  IVIC syndrome
       H02324  Sacral agenesis with vertebral anomalies
       H02327  KBG syndrome
       H02328  Sifrim-Hitz-Weiss syndrome
       H02334  Pierpont syndrome
       H02364  Heart and brain malformation syndrome
       H02368  Developmental delay with short stature, dysmorphic facial features, and sparse hair
       H02369  IMAGE-I syndrome
       H02370  FILS syndrome
       H02376  Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies
       H02381  Cleft palate, psychomotor retardation, and distinctive facial features
       H02382  Bainbridge-Ropers syndrome
       H02383  Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
       H02391  Infantile-onset multisystem neurologic, endocrine, and pancreatic disease
       H02394  Cleft palate, cardiac defects, and mental retardation
       H02453  Congenital heart defects and ectodermal dysplasia
       H02454  Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
       H02455  Congenital heart defects, hamartomas of tongue, and polysyndactyly
       H02478  CATIFA syndrome
       H02479  Nivelon-Nivelon-Mabille syndrome
       H02481  Syndromic disorder with short stature
       H02482  ROSAH syndrome
       H02483  Basel-Vanagaite-Smirin-Yosef syndrome
       H02493  Al Kaissi syndrome
       H02496  Cerebellar, ocular, craniofacial, and genital syndrome
       H02500  Congenital interstitial lung disease with nephrotic syndrome and epidermolysis bullosa
       H02503  Richieri-Costa-Pereira syndrome
       H02506  Cardioacrofacial dysplasia
       H02508  Agenesis of corpus callosum, cardiac, ocular, and genital syndrome
       H02533  Kaufman oculocerebrofacial syndrome
       H02581  Juberg-Hayward syndrome
       H02595  Oculoskeletodental syndrome
       H02607  Short stature and microcephaly with genital anomalies
       H02619  Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
       H02625  Primordial dwarfism-immunodeficiency-lipodystrophy syndrome
       H02641  Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
       H02650  Menke-Hennekam syndrome
       H02694  Alazami-Yuan syndrome
       H02725  Heart-hand syndrome
       H02876  Cantu syndrome
       H02884  RHYNS syndrome
       H02926  Elsahy-Waters syndrome
       H02927  DEEAH syndrome
       H02943  Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome
       H02953  Uruguay facio-cardio-musculo-skeletal syndrome
       H03039  Short stature-micrognathia syndrome
       H03092  CDAGS syndrome
       H03093  Abruzzo-Erickson syndrome
       H03094  Meacham syndrome
       H01824  CODAS syndrome
       H01850  Hartsfield syndrome
       H01857  Filippi syndrome
       H02343  EVEN-plus syndrome
       H02465  Weiss-Kruszka syndrome
       H02547  BRENS syndrome
       H02548  CIMDAG syndrome
       H02549  Cerebellar ataxia, brain abnormalities, and cardiac conduction defects
       H02578  Short stature, microcephaly, and endocrine dysfunction
       H02638  Zaki syndrome
       H02639  Atelis syndrome
       H02663  Braddock-Carey syndrome
       H02667  Takenouchi-Kosaki syndrome
       H02710  Yuksel-Vogel-Bauer syndrome
       H02733  Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies
       H02747  Oculogastrointestinal neurodevelopmental syndrome
       H02748  Hepatorenocardiac degenerative fibrosis
       H02753  Vertebral anomalies and variable endocrine and T-cell dysfunction
       H02759  Suleiman-El-Hattab syndrome
       H02762  Osteo-oto-hepato-enteric syndrome
       H02763  Neurocardiofaciodigital syndrome
       H02764  Short stature, hearing loss, retinitis pigmentosa, and distinctive facies
       H02772  Neurooculocardiogenitourinary syndrome
       H02780  Liberfarb syndrome
       H02850  TIMES syndrome
       H02851  Muggenthaler-Chowdhury-Chioza syndrome
       H02860  Gillespie syndrome
       H02905  Santos syndrome
       H02910  Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction
       H02950  Spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and Leber congenital amaurosis
       H02961  Guillouet-Gordon syndrome
       H02968  Curry-Jones syndrome
       H02969  Hardikar syndrome
       H02978  FICUS syndrome
       H02981  Neurooculorenal syndrome
       H02982  Congenital heart defects and skeletal malformations syndrome
       H02991  Alsahan-Harris syndrome
       H02996  Neurocardiorenal malformation syndrome
       H03002  Xerosis and growth failure with immune and pulmonary dysfunction syndrome
       H03003  Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis
       H03015  Brain abnormalities, neurodegeneration, and dysosteosclerosis
       H03021  Craniofaciocardiohepatic syndrome
       H03034  Hypopigmentation, organomegaly, and delayed myelination and development
       H03042  Developmental delay, language impairment, and ocular abnormalities
       H03063  Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness
       H03066  Craniofacial anomalies and anterior segment dysgenesis syndrome
       H03076  Ayme-Gripp syndrome
       H03079  Posterior amelia with pelvic and pulmonary hypoplasia syndrome
       H03101  Lung-brain developmental disorder

     H01732  Angelman syndrome
     H02976  Waisman syndrome
     H00478  Prader-Willi syndrome
     H00440  Rett syndrome
     H00597  Snyder-Robinson syndrome
     H00769  Hyperekplexia
     H00940  Cohen syndrome
     H01769  ZTTK syndrome
     H01913  Renpenning syndrome
     H01914  Christianson syndrome
     H01916  Stocco dos Santos X-linked mental retardation syndrome
     H01920  Partington syndrome
     H01922  Infantile hypotonia with psychomotor retardation and characteristic facies
     H01928  Smith-Kingsmore syndrome
     H02137  Laurence-Moon syndrome
     H02252  PEHO syndrome
     H02305  RERE-related neurodevelopmental syndrome
     H02325  Schaaf-Yang syndrome
     H02337  Skraban-Deardorff syndrome
     H02338  PEHO-like syndrome
     H02346  Intellectual developmental disorder with short stature
     H02353  Hyperekplexia and epilepsy
     H02363  Ververi-Brady syndrome
     H02365  Helsmoortel-van der Aa syndrome
     H02378  Hypotonia, ataxia, and delayed development syndrome
     H02397  Neurodevelopmental disorder with movement abnormalities or hypotonia
     H02437  Growth retardation, impaired intellectual development, hypotonia, and hepatopathy
     H02459  Syndromic neurodevelopmental disorder
     H02460  Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies
     H02461  Neurodevelopmental disorder with microcephaly
     H02463  Syndromic intellectual developmental disorder
     H02470  Neurodevelopmental disorder with structural brain abnormalities
     H02510  Neurodevelopmental disorder with characteristic facial and ectodermal features and tetraparesis
     H02515  Li-Ghorbani-Weisz-Hubshman syndrome
     H02528  Hao-Fountain syndrome
     H02535  Neurodevelopmental disorder with dysmorphic facies
     H02560  White-Kernohan syndrome
     H02582  Mullegama-Klein-Martinez syndrome
     H02583  X-linked intellectual disability-hypotonic facies syndrome
     H02584  Ferguson-Bonni neurodevelopmental syndrome
     H02587  Luo-Schoch-Yamamoto syndrome
     H02611  Turnpenny-Fry syndrome
     H02612  Radio-Tartaglia syndrome
     H02613  Brunet-Wagner neurodevelopmental syndrome
     H02614  Snijders Blok-Campeau syndrome
     H02615  Parenti-Mignot neurodevelopmental syndrome
     H02616  Neurodevelopmental disorder with macrocephaly
     H02617  Bryant-Li-Bhoj neurodevelopmental syndrome
     H02618  Developmental delay with variable intellectual disability and dysmorphic facies
     H02622  Shukla-Vernon syndrome
     H02623  Kury-Isidor syndrome
     H02632  Houge-Janssens syndrome
     H02633  Beck-Fahrner syndrome
     H02635  Poirier-Bienvenu neurodevelopmental syndrome
     H02651  Lessel-Kreienkamp syndrome
     H02659  Dentici-Novelli neurodevelopmental syndrome
     H02666  Chilton-Okur-Chung neurodevelopmental syndrome
     H02682  Nizon-Isidor syndrome
     H02685  Developmental delay with neuropsychiatric disorders
     H02686  Developmental delay with dysmorphic facies and dental anomalies
     H02688  Dworschak-Punetha neurodevelopmental syndrome
     H02698  Trichohepatoneurodevelopmental syndrome
     H02700  Intellectual developmental disorder with speech delay and dysmorphic facies
     H02712  Li-Campeau syndrome
     H02714  Tessadori-Bicknell-van Haaften neurodevelopmental syndrome
     H02715  Neurodevelopmental disorder with defects of ubiquitin-proteasome system
     H02728  Marbach-Schaaf neurodevelopmental syndrome
     H02734  Hengel-Maroofian-Schols syndrome
     H02746  Alfadhel syndrome
     H02752  Tan-Almurshedi syndrome
     H02765  Prieto syndrome
     H02769  Tolchin-Le Caignec syndrome
     H02782  Fliedner-Zweier syndrome
     H02793  Temtamy syndrome
     H02803  Neurodevelopmental disorder with histone modification defect
     H02804  ReNU syndrome
     H02812  Otofacial neurodevelopmental syndrome
     H02818  Jeffries-Lakhani neurodevelopmental syndrome
     H02824  Abnormal hair, joint laxity, and developmental delay
     H02834  Kariminejad-Reversade neurodevelopmental syndrome
     H02837  Karayol-Borroto-Haghshenas neurodevelopmental syndrome
     H02838  Neurodevelopmental disorder with variable familial hypercholanemia
     H02842  Pan-Chung-Bellen syndrome
     H02843  Brain malformations and seizures by impaired function of TRiC
     H02854  Okur-Chung neurodevelopmental syndrome
     H02855  Shashi-Pena syndrome
     H02856  Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
     H02857  Neurodevelopmental disorder with microcephaly and structural brain anomalies
     H02858  Neurodevelopmental disorder with speech impairment and with or without seizures
     H02859  Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
     H02861  Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures
     H02862  Neurodevelopmental disorder with or without variable brain abnormalities
     H02863  Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
     H02864  Neurodevelopmental disorder with or without autism or seizures
     H02885  Neurodevelopmental disorder with hypotonia and dysmorphic facies
     H02886  Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities
     H02887  Neurodevelopmental disorder with language impairment and behavioral abnormalities
     H02888  Neurodevelopmental disorder with or without seizures and gait abnormalities
     H02890  Neurodevelopmental disorder with language delay and variable cognitive abnormalities
     H02891  Neurodevelopmental disorder with poor language and loss of hand skills
     H02892  Neurodevelopmental disorder with infantile epileptic spasms
     H02894  Neurodevelopmental disorder with impaired language and ataxia and with or without seizures
     H02911  Paul-Chao neurodevelopmental syndrome
     H02918  Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
     H02924  Intellectual disability and myopathy syndrome
     H02933  Delpire-McNeill syndrome
     H02934  Kilquist syndrome
     H02959  Li-Takada-Miyake syndrome
     H02965  Hoxha-Aliu syndrome
     H02974  Blepharophimosis-impaired intellectual development syndrome
     H02983  Leukodystrophy and cerebellar atrophy
     H02984  Clark-Baraitser syndrome
     H02986  Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
     H02987  Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
     H02988  Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity
     H02992  Neurodevelopmental disorder with achalasia, polyneuropathy, and alacrima
     H02993  Developmental delay, dysmorphic facies, and brain anomalies
     H02994  Neurodevelopmental disorder with growth impairment, quadriparesis, and poor or absent speech
     H02995  Harel-Tora neurodevelopmental syndrome
     H02997  Neurodevelopmental disorder with seizures and joint laxity
     H02998  Neurodevelopmental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities
     H03001  Dursun-Ozgul neurodevelopmental syndrome
     H03006  Rabin-Pappas syndrome
     H03010  Neurodevelopmental disorder with absent language and variable seizures
     H03011  Congenital hypotonia, epilepsy, developmental delay, and digital anomalies
     H03017  Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects
     H03018  Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities
     H03019  Neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures
     H03026  Neurodevelopmental disorder with hypotonia, epilepsy, and absent speech
     H03027  Neurodevelopmental disorder with speech delay, movement abnormalities, and seizures
     H03028  Intellectual development disorder with seizures and dysmorphic facies
     H03032  Ramond-Elliott neurodevelopmental syndrome
     H03035  Halperin-Birk syndrome
     H03038  Pettigrew syndrome
     H03040  Neurodevelopmental disorder with epilepsy and brain atrophy
     H03041  Neurodevelopmental disorder with poor growth and skeletal anomalies
     H03043  Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies
     H03044  Neurodevelopmental disorder with structural brain abnormalities and craniofacial abnormalities
     H03045  Neurodevelopmental disorder with parkinsonism or other movement abnormalities
     H03046  Intellectual developmental disorder with poor growth and with or without seizures or ataxia
     H03071  Davis-Wells syndrome
     H03077  Developmental delay, impaired speech, and behavioral abnormalities
     H03085  Popov-Chang syndrome
     H03088  Neurodevelopmental disorder with spasticity, hypoplasia of the corpus callosum, and recurrent infections
     H03095  Neurodevelopmental disorder with microcephaly and movement abnormalities
     H03100  Damseh-Danson neurodevelopmental disorder
     H03102  STAD syndrome
     H03108  Developmental delay with variable cardiac and renal congenital anomalies and dysmorphic facies

     MB20  Symptoms, signs or clinical findings involving consciousness
     MB21  Symptoms, signs or clinical findings involving cognition
     MB22  Symptoms or signs involving motivation or energy
     MB23  Symptoms or signs involving appearance or behaviour
     MB24  Symptoms or signs involving mood or affect
     MB25  Symptoms or signs involving form of thought
     MB26  Symptoms or signs involving content of thought
     MB27  Symptoms or signs involving perceptual disturbance
     MB28  Symptoms or signs related to personality features
     MB29  Symptoms or signs involving eating and related behaviour
     MB2A  Symptoms or signs involving elimination
     MB2Y  Other specified mental or behavioural symptoms, signs or clinical findings

         MD90  Nausea or vomiting
         MD91  Belching
         MD92  Dyspepsia
         MD93  Dysphagia
         MD94  Halitosis
         MD95  Heartburn
         MD9Y  Other specified symptoms related to the upper gastrointestinal tract

         ME00  Abdominal compartment syndrome
         ME01  Abdominal distension
         ME02  Abdominal rigidity
         ME03  Abnormal bowel sounds
         ME04  Ascites
         ME05  Change in bowel habit
         ME06  Chronic enteritis of uncertain aetiology
         ME07  Faecal incontinence
         ME08  Flatulence or related conditions
         ME09  Rectal tenesmus
         ME0A  Visible peristalsis
         ME0B  Problems with defaecation, not otherwise specified
         ME0Y  Other specified symptoms related to the lower gastrointestinal tract or abdomen

       ME60  Skin lesion of uncertain or unspecified nature
       ME61  Subcutaneous swelling, mass or lump of uncertain or unspecified nature
       ME62  Acute skin eruption of uncertain or unspecified nature
       ME63  Chronic skin disorder of uncertain or unspecified nature
       ME64  Non-specific cutaneous vascular signs
       ME65  Disturbances of skin sensation of unspecified aetiology
       ME66  Miscellaneous non-specific skin-related symptoms or signs
       ME67  Skin disorder of uncertain or unspecified nature
       ME6Y  Other specified symptoms or signs involving the skin