- OMIM ID
-
269880
- OMIM term:
- SHORT SYNDROME
- Alternative terms:
-
SHORT STATURE, HYPEREXTENSIBILITY, HERNIA, OCULAR DEPRESSION, RIEGER ANOMALY, AND TEETHING DELAY
LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, AND SHORT STATURE
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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