Lissencephaly with cerebellar hypoplasia type C

Orpha code: 100013OMIM code:

Definition

A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death.

Disease data
Classification

Malformation syndrome

ORPHA code
100013
OMIM code
-
ICD10 code
Q04.3
ICD11 code
-

No additional description.

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