Mental retardation, autosomal recessive 8

Preferred Label : Mental retardation, autosomal recessive 8;

Obsolete resource : true;

Moved to : 614300;

Alternative titles and symbols : Mrt8;

Prefixed ID : 611094;

Details

Origin ID

611094;

UMLS CUI

C1970196;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive non-syndromic intellectual disability [ORDO Disease]
Currated CISMeF NLP mapping
- mental retardation, autosomal recessive 8 [MeSH concept]
- mental retardation, autosomal recessive 8 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, autosomal recessive 8 [MeSH Supplementary Concept]
- mental retardation, autosomal recessive 8 [MeSH concept]

Keyword's position in hierarchy(ies) :

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