Hypercalcemia, infantile, 2

MONDO:0014851

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

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

1 clinical trial for this condition and its sub-types, 0 tagged with Hypercalcemia, infantile, 2 itself.

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↑ Hypercalcemia, infantile (2)

Including sub-types (1) Tagged with Hypercalcemia, infantile, 2 (0)

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