 01 Certain infectious or parasitic diseases
|
|
02 Neoplasms
|
|
03 Diseases of the blood or blood-forming organs
|
|
04 Diseases of the immune system
|
|
05 Endocrine, nutritional or metabolic diseases
|
|
06 Mental, behavioural or neurodevelopmental disorders
|
|
07 Sleep-wake disorders
|
|
08 Diseases of the nervous system
|
|
09 Diseases of the visual system
|
|
10 Diseases of the ear or mastoid process
|
|
11 Diseases of the circulatory system
|
|
12 Diseases of the respiratory system
|
|
13 Diseases of the digestive system
|
|
14 Diseases of the skin
|
|
15 Diseases of the musculoskeletal system or connective tissue
|
|
16 Diseases of the genitourinary system
|
|
17 Conditions related to sexual health
|
|
18 Pregnancy, childbirth or the puerperium
|
|
19 Certain conditions originating in the perinatal period
|
|
 20 Developmental anomalies
|
Structural developmental anomalies primarily affecting one body system
|
Multiple developmental anomalies or syndromes
|
LD20 Syndromes with central nervous system anomalies as a major feature
|
LD21 Syndromes with eye anomalies as a major feature
|
 LD22 Syndromes with dental anomalies as a major feature
|
LD23 Syndromes with vascular anomalies as a major feature
|
LD24 Syndromes with skeletal anomalies as a major feature
|
LD25 Syndromes with face or limb anomalies as a major feature
|
LD26 Syndromes with limb anomalies as a major feature
|
LD27 Syndromes with skin or mucosal anomalies as a major feature
|
LD28 Syndromes with connective tissue involvement as a major feature
|
LD29 Syndromes with obesity as a major feature
|
LD2A Malformative disorders of sex development
|
H00607 46,XY 性腺形成不全症
H00608 46,XY性分化疾患 (テストステロン分泌異常)
H02177 アンドロゲン不応症
H00442 屈曲肢異形成
H00598 46,XX 精巣性分化疾患
H00609 ミュラー管遺残症候群
H02317 SERKAL 症候群
H02318 皮膚有棘細胞癌と性転換を伴う掌蹠角化症
|
LD2B Syndromes with premature ageing appearance as a major feature
|
LD2C Overgrowth syndromes
|
LD2D Phakomatoses or hamartoneoplastic syndromes
|
LD2E Syndromes with structural anomalies due to inborn errors of metabolism
|
LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
|
LD2G Conjoined twins
|
LD2H Syndromic genetic deafness
|
LD2Y Other specified multiple developmental anomalies or syndromes
|
LD2Z Multiple developmental anomalies or syndromes, unspecified
|
Chromosomal anomalies, excluding gene mutations
|
LD90 Conditions with disorders of intellectual development as a relevant clinical feature
|
LD9Y Other specified developmental anomalies
|
LD9Z Developmental anomalies, unspecified
|
|
21 Symptoms, signs or clinical findings, not elsewhere classified
|
|
22 Injury, poisoning or certain other consequences of external causes
|
ICD-11 による疾患分類