Ectodermal dysplasia syndrome, unspecified

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LD27.00 – Incontinentia pigmenti
LD27.01 – Cronkhite-Canada syndrome
LD27.02 – Hypohidrotic ectodermal dysplasia
LD27.03 – Hidrotic ectodermal dysplasia, Clouston type
LD27.0Y – Other specified ectodermal dysplasia syndromes

Foundation entity

Ectodermal dysplasia syndromes – http://id.who.int/icd/entity/1156567558

Part of: LD27.0: Ectodermal dysplasia syndromes › LD27: Syndromes with skin or mucosal anomalies as a major feature › 20: Developmental anomalies