Autosomal dominant hypocalcemia 2

Definition

An autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Also known as autosomal dominant hypocalcemia type 2, HYPOC2, hypocalcemia, autosomal dominant type 2 — per MONDO

Also identified as

• DOID 0090108 per MONDO
• OMIM 615361 per MONDO
• UMLS C3809243 per MONDO