Syndromes with multiple structural anomalies, without predominant body system involvement

Child codes

• LD2F.0 – Toxic or drug-related embryofetopathies
• LD2F.1 – Syndromes with multiple structural anomalies, not of environmental origin
• LD2F.Y – Other specified syndromes with multiple structural anomalies, without predominant body system involvement
• LD2F.Z – Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified

Foundation children elsewhere

• 5C50.02 – Embryofetopathy due to maternal phenylketonuria
• KA62.0 – Congenital Zika virus infection
• KA62.1 – Congenital Epstein-Barr virus infection
• KA62.2 – Congenital Varicella Zoster virus infection
• KA62.3 – Congenital cytomegalovirus infection
• KA62.5 – Congenital enterovirus infection
• KA62.7 – Congenital parvovirus syndrome
• KA62.8 – Congenital rubella syndrome
• KA62.A – Perinatal Herpes simplex infection
• KA64.0 – Congenital toxoplasmosis

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
• LD2A – Malformative disorders of sex development
• 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
• LD2G – Conjoined twins
• LD2H – Syndromic genetic deafness
• LD2Y – Other specified multiple developmental anomalies or syndromes
• LD2Z – Multiple developmental anomalies or syndromes, unspecified

Foundation entity

Syndromes with multiple structural anomalies, without predominant body system involvement – http://id.who.int/icd/entity/1953029110