polycystic kidney, autosomal dominant

Preferred Label : polycystic kidney, autosomal dominant;

MeSH definition : Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function.;

MeSH synonym : polycystic kidney disease, autosomal dominant; autosomal dominant polycystic kidney; adult polycystic kidney disease; kidney, polycystic, autosomal dominant; adpkd; polycystic kidney disease, adult;

MeSH hyponym : polycystic kidney, type 1 autosomal dominant disease; polycystic kidney, type 2 autosomal dominant disease; Polycystic Kidney Disease, Adult, Type II; Polycystic Kidney Disease, Type 2; Polycystic Kidney Disease, Adult Type 2; Adult Polycystic Kidney Disease Type 2; Polycystic Kidney Disease 2; Adult Polycystic Kidney Disease Type 1;

Details

Origin ID

D016891;

UMLS CUI

C0085413;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Adult type polycystic kidney disease type 1 (disorder) [SNOMED CT concept]
- Adult type polycystic kidney disease type 2 (disorder) [SNOMED CT concept]
- Autosomal Dominant Polycystic Kidney Disease Type I [NCIt concept]
- Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis [ICD-11 More detail]
- Autosomal dominant polycystic kidney disease, Type 2 [ICD-11 More detail]
- PKD1 Gene [NCIt concept]
- polycystic kidney disease 2 [DO Concept]
Currated CISMeF NLP mapping
- Autosomal Dominant Polycystic Kidney Disease [NCIt concept]
- Autosomal dominant polycystic kidney disease [ICD-11 Category]
- Autosomal dominant polycystic kidney disease [ORDO Disease]
- Autosomal dominant polycystic kidney disease (disorder) [SNOMED CT concept]
- Polycystic kidney disease 1 with or without polycystic liver disease [OMIM Phenotype]
- Polycystic kidney disease, adult type (disorder) [Inactive SNOMED CT concept]
- Polycystic kidney, adult type [ICD-10 Sub-category]
- Polycystic kidney, adult type [ICD-10 Sub-category (who)]
- Polycystic kidney, autosomal dominant [ICD-9 code]
- Polycystic kidney, autosomal dominant [MedDRA LLT]
- autosomal dominant polycystic kidney disease [DO Concept]
- autosomal dominant polycystic kidney disease [Disease (Nov.)]
Indexing information
- CYS1 protein, human [MeSH Supplementary Concept]
- Cys1 protein, mouse [MeSH Supplementary Concept]
- polycystic kidney disease 1 protein [MeSH Supplementary Concept]
- polycystic kidney disease 2 protein [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Channelopathy due to a transient receptor potential channel defect [ORDO Disease]
- Male infertility due to obstructive azoospermia [ORDO Disease]
Record concept(s)
- polycystic kidney, autosomal dominant [MeSH concept]
- polycystic kidney, type 1 autosomal dominant disease [MeSH concept]
- polycystic kidney, type 2 autosomal dominant disease [MeSH concept]
Related MeSH Supplementary Concept(s)
- medullary cystic kidney disease 1 [MeSH Supplementary Concept]
- medullary cystic kidney disease 2 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal Dominant Polycystic Kidney Disease [NCIt concept]
- Autosomal dominant polycystic kidney disease (disorder) [SNOMED CT concept]
- Polycystic kidney disease, adult type (disorder) [Inactive SNOMED CT concept]
- Polycystic kidney, adult type [ICD-10 Sub-category]
- Polycystic kidney, autosomal dominant [MedDRA LLT]
- Polycystic kidney, autosomal dominant [ICD-9 code]
- polycystic kidney disease, adult type [SNOMED Notion]
Validated automatic mappings to BTNT
- Autosomal Dominant Polycystic Kidney Disease Type 2 [NCIt concept]
- Polycystic kidney disease 2 with or without polycystic liver disease [OMIM Phenotype]

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