All diseases

OMIM ID
146200
OMIM term:
HYPOPARATHYROIDISM, FAMILIAL ISOLATED; FIH
Alternative terms:
HYPOPARATHYROIDISM, AUTOSOMAL DOMINANT
HYPOCALCEMIA, AUTOSOMAL DOMINANT
HYPOCALCEMIA, FAMILIAL
HYPERCALCIURIC HYPOCALCEMIA, FAMILIAL HYPOPARATHYROIDISM, AUTOSOMAL RECESSIVE, INCLUDED
(∗) Location:
11p15.2   3q21.1   6p24.2  
(†) Associated OMIM genes:
CASR   GCM2   PTH  
(‡) Associated MGI genes:
Gcm2  

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