Search Ontology:
Human Disease
infantile hypercalcemia 2
- Term ID
- DOID:0061135
- Synonyms
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- Definition
- A hypercalcemia that has_material_basis_in homozygous or compound heterozygous mutation in the SLC34A1 gene on chromosome 5q35. https://pubmed.ncbi.nlm.nih.gov/26047794/
- References
- Ontology
- Human Disease ( DOID:0061135 )
- is a type of
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