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familial hypoparathyroidism

Disease Summary
Associated Targets (4)
Tbio

2

Tclin

1

Tchem

1


GARD Rare
Mondo Description A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects.
Mondo Term and Equivalent IDs
MONDO:0016390:  familial hypoparathyroidism
DOID:0111387: 
GARD:0002910: 
MESH:C537156: 
OMIMPS:146200: 
Orphanet:2238: 
SCTID:725036000: 
UMLS:C1832648: