Intellectual developmental disorder, autosomal recessive 4

Preferred Label : Intellectual developmental disorder, autosomal recessive 4;

Symbol : MRT4;

CISMeF acronym : MRT4;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Mental retardation, autosomal recessive 4;

Inheritance : Autosomal recessive;

Prefixed ID : %611107;

Details

Origin ID

611107;

UMLS CUI

C1970179;

Currated CISMeF NLP mapping
- mental retardation, autosomal recessive 4 [MeSH concept]
- mental retardation, autosomal recessive 4 [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive non-syndromic intellectual disability [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Delayed myelination [HPO term]
- Global developmental delay [HPO term]
- Intellectual disability [HPO term]
- Malar flattening [HPO term]
- Microcephaly [HPO term]
- Upslanted palpebral fissure [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 4 [MeSH Supplementary Concept]
- mental retardation, autosomal recessive 4 [MeSH concept]

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