Familial hypocalciuric hypercalcemia 2

Definition

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

Also known as familial hypocalciuric hypercalcemia type 2, FHH type 2, HHC2, hpocalciuric hypercalcemia, type II — per MONDO

Also identified as

• DOID 0060701 per MONDO
• MESH C537146 per MONDO
• OMIM 145981 per MONDO
• Orphanet 101049 per MONDO
• UMLS C1840347 per MONDO