- OMIM ID
-
300067
- OMIM term:
- LISSENCEPHALY, X-LINKED, 1; LISX1
- Alternative terms:
-
XLIS
LISSENCEPHALY AND AGENESIS OF CORPUS CALLOSUM SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED; SCLH, INCLUDED
SUBCORTICAL BAND HETEROTOPIA, X-LINKED, INCLUDED; SBH, INCLUDED
DOUBLE CORTEX SYNDROME, INCLUDED
DC SYNDROME, INCLUDED
- (∗) Location:
- Xq23
- (†) Associated OMIM genes:
- DCX
- (‡) Associated MGI genes:
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