Intellectual developmental disorder, X-linked 2

Preferred Label : Intellectual developmental disorder, X-linked 2;

Symbol : XLID2;

CISMeF acronym : MRX2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRX2; Mental retardation, X-linked 2;

Inheritance : X-linked;

Prefixed ID : %300428;

Details

Origin ID

300428;

UMLS CUI

C0796207;

Currated CISMeF NLP mapping
- mental retardation, X-Linked 2 [MeSH concept]
- mental retardation, X-Linked 2 [MeSH Supplementary Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability 2 [DO Concept]
HPO term(s)
- High palate [HPO term]
- Intellectual disability [HPO term]
- Macroorchidism [HPO term]
- Poor fine motor coordination [HPO term]
- Relative macrocephaly [HPO term]
- Short stature [HPO term]
- Square face [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- X-linked non-syndromic intellectual disability [ORDO Disease]
See also inter- (CISMeF)
- PQBP1 wt Allele [NCIt concept]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, X-Linked 2 [MeSH Supplementary Concept]
- mental retardation, X-Linked 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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