Lissencephaly with cerebellar hypoplasia type F

Orpha code: 100016OMIM code:

Definition

A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum.

Disease data
Classification

Malformation syndrome

ORPHA code
100016
OMIM code
-
ICD10 code
Q04.3
ICD11 code
-

No additional description.

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