ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD25 — Syndromes with face or limb anomalies as a major feature
LD25.0 — Oromandibular-limb anomaly syndrome
LD25.00 — Oral-facial-digital syndrome

ICD-11 LD25.00 — Oral-facial-digital syndrome

A condition caused by failure of the head and digits to correctly develop during the antenatal period. This condition may be associated with cleft or lobed tongue, noncancerous tumours or nodules of the tongue, abnormal shape or number of teeth, cleft palate, hyperplastic frenula of the lip or gums, cleft lip, hypertelorism, wide nose with broad, flat nasal bridge, syndactyly, brachydactyly, clinodactyly, polydactyly, polycystic kidney disease, neurological problems, bone abnormalities, vision loss, or heart defects.

The diagnosis includes nothing.

The diagnosis excludes nothing.

It has no clarifying diagnoses.

The diagnosis is coded elsewhere:

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