Intellectual developmental disorder, X-linked 88

Preferred Label : Intellectual developmental disorder, X-linked 88;

Symbol : XLID88;

CISMeF acronym : MRX88;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MRX88; Mental retardation, X-linked 88;

Inheritance : X-linked;

Prefixed ID : %300852;

Details

Origin ID

300852;

UMLS CUI

C3275444;

Automatic exact mappings (from CISMeF team)
- AGTR2 wt Allele [NCIt concept]
- X-linked non-syndromic intellectual disability [ORDO Disease]
- angiotensin II receptor type 2 [ORDO Gene]
- angiotensin II receptor type 2 [HGNC gene]
- non-syndromic X-linked intellectual disability 88 [DO Concept]
DO Cross reference
- non-syndromic X-linked intellectual disability 88 [DO Concept]
HPO term(s)
- Autism [HPO term]
- Global developmental delay [HPO term]
- Intellectual disability [HPO term]
- Seizure [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]

Keyword's position in hierarchy(ies) :

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