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Familial Hypocalciuric Hypercalcemia 2 (MONDO:0007792)

A familial hypocalciuric hypercalcemia that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Overview

Category

Ontology ID

Internal:9137

Synonyms

FHH type 2

HHC2

familial hypocalciuric hypercalcemia type 2

hpocalciuric hypercalcemia, type II

FBH2

familial benign hypercalcemia, type 2

hypercalcemia, familial benign type 2

hypercalcemia, familial benign, type 2

hypocalciuric hypercalcemia, familial, type 2

hypocalciuric hypercalcemia, familial, type II

Mapped terms

DOID:0060701

GARD:0009758

MEDGEN:374447

MESH:C537146

OMIM:145981

Orphanet:101049

UMLS:C1840347

Child terms

Unknown children.