Hypercalcemia, infantile, 2

Definition

Any hypercalcemia, infantile in which the cause of the disease is a mutation in the SLC34A1 gene.

Also known as autosomal recessive infantile hypercalcemia caused by mutation in SLC34A1, HCINF2, hypercalcemia, infantile 2, hypercalcemia, infantile, 2, hypercalcemia, infantile, type 2, SLC34A1 autosomal recessive infantile hypercalcemia — per MONDO

Also identified as

• DOID 0061135 per MONDO
• OMIM 616963 per MONDO
• UMLS C4310473 per MONDO