Intellectual developmental disorder, X-linked 95

Preferred Label : Intellectual developmental disorder, X-linked 95;

Symbol : XLID95;

CISMeF acronym : MRX95;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRX95; Mental retardation, X-linked 95;

Inheritance : X-linked dominant;

Prefixed ID : %300716;

Details

Origin ID

300716;

UMLS CUI

C2678034;

Automatic exact mappings (from CISMeF team)
- MAGT1 wt Allele [NCIt concept]
- X-linked non-syndromic intellectual disability [ORDO Disease]
- magnesium transporter 1 [ORDO Gene]
- magnesium transporter 1 [HGNC gene]
Currated CISMeF NLP mapping
- mental retardation, X-Linked 95 [MeSH concept]
- mental retardation, X-Linked 95 [MeSH Supplementary Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability [DO Concept]
HPO term(s)
- Delayed speech and language development [HPO term]
- Intellectual disability [HPO term]
- X-linked dominant inheritance [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]
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- mental retardation, X-Linked 95 [MeSH Supplementary Concept]
- mental retardation, X-Linked 95 [MeSH concept]

Keyword's position in hierarchy(ies) :

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