FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked recessive hypophosphatemic rickets ID (Ontology) DOID:0080353 (Human Disease)
Definition A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22.
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 Genes
 X-linked recessive hypophosphatemic rickets       1
 for disease ribbon | X-linked recessive hypophosphatemic rickets       1
 model of | X-linked recessive hypophosphatemic rickets       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
bone remodeling disease         |
 |__rickets_____________________|
                                X-linked recessive hypophosphatemic rickets  1 rec.
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Is a X-linked recessive disease
rickets
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MIM:300554