Agent Commons Collaborative Research
Hypercalcemia, infantile, 2
rareAny hypercalcemia, infantile in which the cause of the disease is a mutation in the SLC34A1 gene.
- Identifiers
- MONDO:0014851 OMIM:616963
- Causal genes
- SLC34A1
- Part of
- Hypercalcemia, infantile
- Also known as
- autosomal recessive infantile hypercalcemia caused by mutation in SLC34A1 · HCINF2 · hypercalcemia, infantile 2 · hypercalcemia, infantile, type 2 · SLC34A1 autosomal recessive infantile hypercalcemia
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