polycystic kidney diseases

Preferred Label : polycystic kidney diseases;

MeSH definition : Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance.;

MeSH synonym : kidney disease, polycystic; polycystic kidney disease; renal disease, polycystic; disease, polycystic renal; disease, polycystic kidney; diseases, polycystic kidney; kidney diseases, polycystic; polycystic renal disease; diseases, polycystic renal; polycystic renal diseases; renal diseases, polycystic;

Related MeSH term : kidney, polycystic; Polycystic Kidneys; Polycystic Kidney; Kidneys, Polycystic;

MeSH annotation : KIDNEY, CYSTIC and MULTICYSTIC DYSPLASTIC KIDNEY are also available; prefer specifics;

Details

Origin ID

D007690;

UMLS CUI

C0022680;

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)
- EIF2AK2 wt Allele [NCIt concept]
- Interferon-Induced, Double-Stranded RNA-Activated Protein Kinase [NCIt concept]
- Kidney polycystic [MedDRA LLT]
- PKLR wt Allele [NCIt concept]
- Photorefractive keratectomy (procedure) [SNOMED CT concept]
- Polycystic kidney [PASCAL descriptor]
- Polycystic kidney disease [OMIM phenotypic series]
- Polycystic kidney, unspecified [ICD-10 Sub-category (who)]
- Polycystic kidneys [HRDO Sign]
- Pyruvate Kinase PKLR [NCIt concept]
- kidney cysts [MedlinePlus Topic]
- kidney diseases [MedlinePlus Topic]
- polycystic kidney disease [DO Concept]
- polycystic kidney disease [EMDN type]
Currated CISMeF NLP mapping
- Polycystic Kidney Disease [NCIt concept]
- Polycystic kidney [MedDRA LLT]
- Polycystic kidney dysplasia [HPO term]
- congenital cystic kidney disease [SNOMED Notion]
- kidney polycystic disorder [Disease (Nov.)]
- polycystic kidney disease [Radlex concept]
DO Cross reference
- autosomal dominant polycystic kidney disease [DO Concept]
HPO term
- Polycystic kidney dysplasia [HPO term]
Indexing information
- PKD1L3 protein, human [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- congenital anomaly urinary tract [ICPC-2 Rubric]
MedlinePlus topic(s)
- kidney diseases [MedlinePlus Topic]
Ne pas confondre avec
- multicystic dysplastic kidney [MeSH Descriptor]
Record concept(s)
- kidney, polycystic [MeSH concept]
- polycystic kidney diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- Meckel-Like cerebrorenodigital syndrome [MeSH Supplementary Concept]
- arima syndrome [MeSH Supplementary Concept]
- cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome [MeSH Supplementary Concept]
- daneman davy mancer syndrome [MeSH Supplementary Concept]
- meckel syndrome type 1 [MeSH Supplementary Concept]
- meckel syndrome type 2 [MeSH Supplementary Concept]
- meckel syndrome type 3 [MeSH Supplementary Concept]
- meckel syndrome, type 4 [MeSH Supplementary Concept]
- meckel syndrome, type 5 [MeSH Supplementary Concept]
- meckel syndrome, type 6 [MeSH Supplementary Concept]
- polycystic kidney disease, type 1 [MeSH Supplementary Concept]
- polycystic kidney, cataract, and congenital blindness [MeSH Supplementary Concept]
- potter type III polycystic kidney disease [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Kidney polycystic [MedDRA LLT]
- Polycystic Kidney Disease [NCIt concept]
- Polycystic kidney [MedDRA LLT]
- Polycystic kidney dysplasia [HPO term]
- Polycystic kidney, unspecified [ICD-10 Sub-category]
- Polycystic kidney, unspecified type [MedDRA LLT]
- Polycystic kidney, unspecified type [ICD-9 code]
- autosomal dominant polycystic kidney disease [DO Concept]

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