/hypercalcemia, infantile, 2

hypercalcemia, infantile, 2

Rare Disease

MONDO:0014851

Also Known As

HCINF2SLC34A1 autosomal recessive infantile hypercalcemiaautosomal recessive infantile hypercalcemia caused by mutation in SLC34A1hypercalcemia, infantile 2hypercalcemia, infantile, 2hypercalcemia, infantile, type 2

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

SLC34A1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616963 ↗

GARD

GARD:18435 ↗

Related Diseases

hypercalcemia, infantile, 1

MONDO:0020739

Rare

← Back to All Diseases