Search Ontology:
Human Disease

infantile hypercalcemia 1

Term ID
DOID:0061136
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0061136 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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