Intellectual developmental disorder, autosomal recessive 10

Preferred Label : Intellectual developmental disorder, autosomal recessive 10;

Symbol : MRT10;

CISMeF acronym : MRT10; MRT20;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRT20; Mental retardation, autosomal recessive 20; Intellectual developmental disorder, autosomal recessive 20; Mental retardation, autosomal recessive 10;

Inheritance : Autosomal recessive;

Prefixed ID : %611096;

Details

Origin ID

611096;

UMLS CUI

C1970194;

Currated CISMeF NLP mapping
- mental retardation, autosomal recessive 10 [MeSH concept]
- mental retardation, autosomal recessive 10 [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive non-syndromic intellectual disability [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Intellectual disability, moderate [HPO term]
- Motor delay [HPO term]
- Seizure [HPO term]
ORDO concept(s)
- Autosomal recessive non-syndromic intellectual disability [ORDO Disease]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, autosomal recessive 10 [MeSH Supplementary Concept]
- mental retardation, autosomal recessive 10 [MeSH concept]

Keyword's position in hierarchy(ies) :

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