Indolylacroyl glycinuria with impaired intellectual development

Preferred Label : Indolylacroyl glycinuria with impaired intellectual development;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Indolylacroyl glycinuria with mental retardation;

Inheritance : Autosomal recessive;

Prefixed ID : 243050;

Détails

Origin ID

243050;

UMLS CUI

C1855738;

Currated CISMeF NLP mapping
- indolylacroyl glycinuria with mental retardation [MeSH concept]
- indolylacroyl glycinuria with mental retardation [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Hyperglycinuria [HPO term]
- Intellectual disability [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- indolylacroyl glycinuria with mental retardation [MeSH Supplementary Concept]
- indolylacroyl glycinuria with mental retardation [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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