Intellectual developmental disorder, X-linked 20

Preferred Label : Intellectual developmental disorder, X-linked 20;

Symbol : XLID20;

CISMeF acronym : MRX20;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRX20; Mental retardation, X-linked 20;

Description : Impaired mental functioning occurs as an isolated feature or as part of many syndromes listed in the X-linked catalog. Mental retardation that is not associated with other distinguishing features is referred to as 'nonspecific.' The Human Gene Mapping Nomenclature Committee (Mulley et al., 1992) proposed to designate each newly reported apparently unique X-linked mental retardation (MRX) family with gene symbols (e.g., MRX1, MRX2) if a minimal lod score of 2.0 was demonstrated between the MR locus and 1 or more X chromosome markers.;

Inheritance : X-linked;

Prefixed ID : %300047;

Details

Origin ID

300047;

UMLS CUI

C0796226;

Currated CISMeF NLP mapping
- mental retardation, X-Linked 20 [MeSH concept]
- mental retardation, X-Linked 20 [MeSH Supplementary Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability 20 [DO Concept]
HPO term(s)
- Intellectual disability [HPO term]
- X-linked 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 20 [MeSH Supplementary Concept]
- mental retardation, X-Linked 20 [MeSH concept]

Keyword's position in hierarchy(ies) :

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