- OMIM ID
-
184253
- OMIM term:
- SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE
- Alternative terms:
-
SPONDYLOMETAPHYSEAL DYSPLASIA, SCHMIDT TYPE
SPONDYLOMETAPHYSEAL DYSPLASIA WITH SEVERE GENU VALGUM
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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