Acrorenal syndrome

Preferred Label : Acrorenal syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal dominant;

Prefixed ID : 102520;

Details

Origin ID

102520;

UMLS CUI

C3495490;

Automatic exact mappings (from CISMeF team)
- Acrorenal syndrome [ICD-11 More detail]
CISMeF manual mappings
- Acrorenal syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Acrorenal syndrome [ORDO Disease]
- acrorenal syndrome [DO Concept]
- acrorenal syndrome [MeSH concept]
- acrorenal syndrome [MeSH Supplementary Concept]
DO Cross reference
- acrorenal syndrome [DO Concept]
HPO term(s)
- Abnormal renal morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
- Hand oligodactyly [HPO term]
- Kidney malformation [HPO term]
ORDO concept(s)
- Acrorenal syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Acrorenal syndrome [ORDO Disease]
- Acrorenal syndrome (disorder) [SNOMED CT concept]
- acrorenal syndrome [MeSH Supplementary Concept]
- acrorenal syndrome [MeSH concept]
- acrorenal syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

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