Infundibulopelvic dysgenesis

Preferred Label : Infundibulopelvic dysgenesis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Laboratory abnormalities : Hematuria;

Prefixed ID : 600989;

Details

Origin ID

600989;

UMLS CUI

C1832949;

Currated CISMeF NLP mapping
- Infundibulopelvic stenosis multicystic kidney syndrome (disorder) [SNOMED CT concept]
- Infundibulopelvic stenosis-multicystic kidney syndrome [ORDO Disease]
- infundibulopelvic dysgenesis [MeSH concept]
- infundibulopelvic dysgenesis [MeSH Supplementary Concept]
HPO term(s)
- Abdominal pain [HPO term]
- Autosomal dominant inheritance [HPO term]
- Microscopic hematuria [HPO term]
- Multicystic kidney dysplasia [HPO term]
ORDO concept(s)
- Infundibulopelvic stenosis-multicystic kidney syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Infundibulopelvic stenosis multicystic kidney syndrome (disorder) [SNOMED CT concept]
- Infundibulopelvic stenosis-multicystic kidney syndrome [ORDO Disease]
- infundibulopelvic dysgenesis [MeSH Supplementary Concept]
- infundibulopelvic dysgenesis [MeSH concept]

Keyword's position in hierarchy(ies) :

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