Malformative disorders of sex development

Child codes

• LD2A.0 – Ovotesticular disorder of sex development
• LD2A.1 – 46,XY gonadal dysgenesis
• LD2A.2 – Testicular agenesis
• LD2A.3 – 46,XY disorder of sex development due to a defect in testosterone metabolism
• LD2A.4 – 46,XY disorder of sex development due to androgen resistance
• LD2A.Y – Other specified malformative disorders of sex development
• LD2A.Z – Malformative disorders of sex development, unspecified

Foundation children elsewhere

• 5A71.01 – Congenital adrenal hyperplasia
• 5A71.1 – 46,XX disorders of sex development induced by androgens of maternal origin
• LD56 – Chimaera 46, XX, 46, XY

Sibling codes

• 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
• 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

Foundation entity

Malformative disorders of sex development – http://id.who.int/icd/entity/565049612