Intellectual developmental disorder, X-linked 92

Preferred Label : Intellectual developmental disorder, X-linked 92;

Symbol : XLID92;

CISMeF acronym : MRX92;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Mental retardation, X-linked 92; MRX92;

Inheritance : X-linked recessive;

Prefixed ID : %300851;

Details

Origin ID

300851;

UMLS CUI

C1845144;

Currated CISMeF NLP mapping
- mental retardation, X-Linked 92 [MeSH concept]
- mental retardation, X-Linked 92 [MeSH Supplementary Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability 92 [DO Concept]
HPO term(s)
- Blepharophimosis [HPO term]
- Decreased testicular size [HPO term]
- High myopia [HPO term]
- Intellectual disability [HPO term]
- Short stature [HPO term]
- X-linked inheritance [HPO term]
- X-linked recessive inheritance [HPO term]
ORDO concept(s)
- X-linked non-syndromic intellectual disability [ORDO Disease]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, X-Linked 92 [MeSH Supplementary Concept]
- mental retardation, X-Linked 92 [MeSH concept]

Keyword's position in hierarchy(ies) :

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