H00019  Pancreatic cancer
     H00031  Breast cancer
     H02531  Familial breast-ovarian cancer
     H00238  Fanconi anemia
     H02569  Pulmonary fibrosis and/or bone marrow failure, telomere-related
     H00627  Premature ovarian failure
     H02577  Karyomegalic interstitial nephritis
     H00599  Ovarian dysgenesis
     H00992  Seckel syndrome
     H01428  Xeroderma pigmentosum
     H00076  Cockayne syndrome
     H02570  Cerebro-oculo-facio-skeletal syndrome
     H02576  Familial cutaneous telangiectasia and cancer syndrome

     H00009  Adult T-cell leukemia
     H00020  Colorectal cancer
     H00048  Hepatocellular carcinoma
     H01023  Juvenile polyposis syndrome
     H01024  Hereditary mixed polyposis syndrome
     H00211  Hemochromatosis
     H01619  Primary pulmonary hypertension
     H00801  Familial thoracic aortic aneurysm and dissection
     H00430  Fibrodysplasia ossificans progressiva
     H02452  Muscle hypertrophy
     H00625  Tooth agenesis
     H00632  Heterotaxy
     H00533  Hereditary hemorrhagic telangiectasia
     H00599  Ovarian dysgenesis
     H00482  Brachydactyly
     H00484  Multiple synostosis syndrome
     H00851  Proximal symphalangism
     H00434  Camurati-Engelmann disease
     H00900  Geleophysic dysplasia
     H02543  Acromesomelic dysplasia
     H00778  Tarsal-carpal coalition syndrome
     H00653  Marfan syndrome
     H00800  Loeys-Dietz syndrome
     H00609  Persistent Mullerian duct syndrome
     H02102  Myhre syndrome