Craniofacial conodysplasia

Orpha code: 85168OMIM code:

Definition

Craniofacial conodysplasia is characterised by craniofacial dysplasia, cone-shaped physes of the hands and feet, and neurological manifestations resembling cerebral palsy. It has been described in one family. The syndrome appeared to be transmitted as a dominant trait.

Disease data
Classification

Malformation syndrome

ORPHA code
85168
OMIM code
-
ICD10 code
Q87.5
ICD11 code
-

No additional description.

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