Renal failure, progressive, with hypertension

Preferred Label : Renal failure, progressive, with hypertension;

Symbol : RFH1;

CISMeF acronym : AORF; RFH1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Nephropathy, familial; Renal failure, adult-onset; Nephritis, familial, without deafness or ocular defect; AORF;

Inheritance : Autosomal dominant;

Laboratory abnormalities : Increased serum creatinine; No proteinuria;

Prefixed ID : %161900;

Details

Origin ID

161900;

UMLS CUI

C0403443;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant progressive nephropathy with hypertension [ICD-11 More detail]
Currated CISMeF NLP mapping
- Autosomal dominant progressive nephropathy with hypertension [ORDO Disease]
- Autosomal dominant progressive nephropathy with hypertension (disorder) [SNOMED CT concept]
- Progressive hereditary glomerulonephritis without deafness (disorder) [SNOMED CT concept]
- renal failure, progressive, with hypertension [MeSH concept]
- renal failure, progressive, with hypertension [MeSH Supplementary Concept]
HPO term(s)
- Adult onset [HPO term]
- Autosomal dominant inheritance [HPO term]
- Elevated circulating creatinine concentration [HPO term]
- Hypertension [HPO term]
- Microscopic hematuria [HPO term]
- Nephritis [HPO term]
- Progressive [HPO term]
- Proteinuria [HPO term]
- Renal insufficiency [HPO term]
- Stage 5 chronic kidney disease [HPO term]
ORDO concept(s)
- Autosomal dominant progressive nephropathy with hypertension [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant progressive nephropathy with hypertension [ORDO Disease]
- Progressive hereditary glomerulonephritis without deafness (disorder) [SNOMED CT concept]
- renal failure, progressive, with hypertension [MeSH Supplementary Concept]
- renal failure, progressive, with hypertension [MeSH concept]

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