Glucoglycinuria

Preferred Label : Glucoglycinuria;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 138070;

Details

Origin ID

138070;

UMLS CUI

C0268536;

Currated CISMeF NLP mapping
- Glucoglycinuria (finding) [SNOMED CT concept]
- glucoglycinuria [SNOMED Notion]
- glucoglycinuria [MeSH concept]
- glucoglycinuria [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Glycosuria [HPO term]
- Hyperglycinuria [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glucoglycinuria (finding) [SNOMED CT concept]
- glucoglycinuria [MeSH Supplementary Concept]
- glucoglycinuria [SNOMED Notion]
- glucoglycinuria [MeSH concept]

Keyword's position in hierarchy(ies) :

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