- OMIM ID
-
241410
- OMIM term:
- HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRD
- Alternative terms:
-
HYPOPARATHYROIDISM WITH SHORT STATURE, MENTAL RETARDATION, AND SEIZURES
SANJAD-SAKATI SYNDROME
HYPOPARATHYROIDISM, CONGENITAL, ASSOCIATED WITH DYSMORPHISM, GROWTH RETARDATION, AND DEVELOPMENTAL DELAY
- (∗) Location:
- 1q42.3
- (†) Associated OMIM genes:
- TBCE
- (‡) Associated MGI genes:
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