Familial hypocalciuric hypercalcemia 1

Definition

Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the CASR gene.

Also known as CASR familial hypocalciuric hypercalcemia, familial benign hypercalcemia 1, familial hypocalciuric hypercalcemia caused by mutation in CASR, familial hypocalciuric hypercalcemia type 1, FHH type 1, HHC1, hpocalciuric hypercalcemia, type I — per MONDO

Also identified as

• DOID 0060700 per MONDO
• MESH C537145 per MONDO
• OMIM 145980 per MONDO
• Orphanet 93372 per MONDO
• SCTID 704166007 per MONDO
• UMLS C0342637 per MONDO