- OMIM ID
-
152950
- OMIM term:
- MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR
- Alternative terms:
-
MICROCEPHALY, LYMPHEDEMA, CHORIORETINAL DYSPLASIA SYNDROME
MLCRD SYNDROME
MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION, AUTOSOMAL DOMINANT
CDMMR SYNDROME
LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME
LYMPHEDEMA AND RETINAL FOLDS WITH MICROCEPHALY AND MICROPHTHALMOS
- (∗) Location:
- 10q23.33
- (†) Associated OMIM genes:
- KIF11
- (‡) Associated MGI genes:
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