LD24.0Z

ICD-11 MMS 2026-01

Syndromes with micromelia, unspecified

Exclusions from above levels

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

Sibling codes

LD24.00 – Achondroplasia
LD24.01 – Hypochondroplasia
LD24.02 – Thanatophoric dysplasia
LD24.03 – Diastrophic dysplasia
LD24.04 – Chondrodysplasia punctata
LD24.0Y – Other specified syndromes with micromelia

Foundation entity

Syndromes with micromelia – http://id.who.int/icd/entity/1660235889

Allowed postcoordination axes

Part of: LD24.0: Syndromes with micromelia › LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies