Term Name: infantile hypercalcemia 2
Synonyms:
Definition: A hypercalcemia that has_material_basis_in homozygous or compound heterozygous mutation in the SLC34A1 gene on chromosome 5q35.
Ontology: Human Disease [DOID:0061135]   ( DOID:0061135 )

Relationships
is a type of: autosomal recessive disease hypercalcemia inherited metabolic disorder