- OMIM ID
-
600383
- OMIM term:
- MESOMELIA-SYNOSTOSES SYNDROME
- Alternative terms:
-
CHROMOSOME 8q13 DELETION SYNDROME
MESOMELIC DYSPLASIA WITH ACRAL SYNOSTOSES, VERLOES-DAVID-PFEIFFER TYPE
MESOMELIC DYSPLASIA, SYNDROMIC
- (∗) Location:
- 8q13
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...