FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term infantile hypercalcemia 1 ID (Ontology) DOID:0061136 (Human Disease)
Definition A hypercalcemia that has_material_basis_in homozygous or compound heterozygous mutation in the CYP24A1 gene on chromosome 20q13.
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 Genes
 infantile hypercalcemia 1      11
 for disease ribbon | infantile hypercalcemia 1      11
 model of | infantile hypercalcemia 1      11
Spanning Tree (Parents/Children)
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disease of metabolism
 |__inherited metabolic disorder__
autosomal genetic disease         |
 |__autosomal recessive disease___|
calcium metabolism disease        |
 |__hypercalcemia_________________|
genetic disease                   |
 |__inherited metabolic disorder__|
                                  infantile hypercalcemia 1  11 rec.
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Is a autosomal recessive disease
hypercalcemia
inherited metabolic disorder
Part of
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MIM:143880