Intellectual developmental disorder, X-linked 50

Preferred Label : Intellectual developmental disorder, X-linked 50;

Symbol : XLID50;

CISMeF acronym : MRX50;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : MRX50; Mental retardation, X-linked 50;

Inheritance : X-linked;

Prefixed ID : #300115;

Details

Origin ID

300115;

UMLS CUI

C1848087;

Currated CISMeF NLP mapping
- mental retardation, X-Linked 50 [MeSH concept]
- mental retardation, X-Linked 50 [MeSH Supplementary Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability 50 [DO Concept]
Genes related to phenotype
- Synapsin I [OMIM gene]
HPO term(s)
- Intellectual disability, mild [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- X-linked non-syndromic intellectual disability [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, X-Linked 50 [MeSH Supplementary Concept]
- mental retardation, X-Linked 50 [MeSH concept]

Keyword's position in hierarchy(ies) :

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