hypercalcemia, infantile, 2

Rare Disease

MONDO:0014851

Also known as:

HCINF2SLC34A1 autosomal recessive infantile hypercalcemiaautosomal recessive infantile hypercalcemia caused by mutation in SLC34A1

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

Genes

Clinical Trials

–

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Report Generation Failed

We couldn't automatically generate the report. This may be due to temporary service issues.

Need this data in your product?

Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.

Explore API Start Free

← Back to All Diseases

Companies Active in hypercalcemia, infantile, 2

1 company

Organizations with orphan designations or approved therapies for this disease

Amgen Inc

Other

Designated

View all companies