FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Dent disease 2 ID (Ontology) DOID:0081454 (Human Disease)
Definition A Dent disease that is characterized by low molecular weight proteinuria and other features of Fanconi syndrome but typically do not include proximal renal tubular acidosis and that has_material_basis_in mutation in the OCRL gene on chromosome Xq26.
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 Genes
 Dent disease 2       1
 for disease ribbon | Dent disease 2       1
 model of | Dent disease 2       1
Spanning Tree (Parents/Children)
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X-linked recessive disease_______
renal tubular transport disease__|
                                 Dent disease
                                  |__Dent disease 2  1 rec.
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Synonyms
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MESH:C564487
MIM:300555
SNOMEDCT_US_2023_03_01:717790004
UMLS_CUI:C1845167