FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant polycystic kidney disease ID (Ontology) DOID:898 (Human Disease)
Definition A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion.
Also Known As "ADPKD" ; "Congenital biliary ectasias" ; "POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1"
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DO.org
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       2
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 autosomal dominant polycystic kidney disease       2      1      1
 model of | autosomal dominant polycystic kidney disease       2       --       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
cystic kidney disease           |
 |__polycystic kidney disease___|
                                autosomal dominant polycystic kidney disease  12 rec.
                                 |__polycystic kidney disease 1 5 rec.
                                 |__polycystic kidney disease 2 3 rec.
                                 |__polycystic kidney disease 3 1 rec.
                                 |__polycystic kidney disease 6 1 rec.
                                 |__polycystic kidney disease 7 1 rec.
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Is a autosomal dominant disease
polycystic kidney disease
Part of
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Synonyms
  • "ADPKD" EXACT OMO:0003012
    "Congenital biliary ectasias" EXACT
    "POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1" EXACT
Secondary IDs
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GARD:10413
ICD10CM:Q61.3
ICD9CM:753.12
MESH:D007690
NCI:C75464
ORDO:730
SNOMEDCT_US_2023_03_01:204955006
UMLS_CUI:C0022680