Craniofacial conodysplasia

Orpha code: 85168OMIM code:

Definicja

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
Klasyfikacja

Malformation syndrome

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

No additional description.

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