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Metadata
ID	DOID:0061136
Name	infantile hypercalcemia 1
Definition	A hypercalcemia that has_material_basis_in homozygous or compound heterozygous mutation in the CYP24A1 gene on chromosome 20q13. https://pubmed.ncbi.nlm.nih.gov/21675912/
Xrefs	MIM:143880
Parent Relationships	is_a hypercalcemia is_a inherited metabolic disorder is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance