Intellectual developmental disorder, autosomal recessive 9

Preferred Label : Intellectual developmental disorder, autosomal recessive 9;

Symbol : MRT9;

CISMeF acronym : MRT26; MRT9;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRT26; Mental retardation, autosomal recessive 26; Intellectual developmental disorder, autosomal recessive 26; Mental retardation, autosomal recessive 9;

Inheritance : Autosomal recessive;

Prefixed ID : %611095;

Details

Origin ID

611095;

UMLS CUI

C1970195;

Currated CISMeF NLP mapping
- mental retardation, autosomal recessive 9 [MeSH concept]
- mental retardation, autosomal recessive 9 [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive non-syndromic intellectual disability [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Growth delay [HPO term]
- Intellectual disability [HPO term]
- Intellectual disability, severe [HPO term]
- Motor delay [HPO term]
- Spasticity [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 9 [MeSH Supplementary Concept]
- mental retardation, autosomal recessive 9 [MeSH concept]
Validated automatic mappings to NTBT
- Autosomal recessive non-syndromic intellectual disability [ORDO Disease]

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