Intellectual developmental disorder, X-linked, syndromic 9

Preferred Label : Intellectual developmental disorder, X-linked, syndromic 9;

Symbol : MRXS9;

CISMeF acronym : MRXS9;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Mental retardation, X-linked, syndromic 9;

Prefixed ID : %300709;

Details

Origin ID

300709;

UMLS CUI

C2678039;

Automatic exact mappings (from CISMeF team)
- Renpenning syndrome 2 [HGNC gene]
- mental retardation, X-Linked 9 [MeSH Supplementary Concept]
- mental retardation, X-Linked 9 [MeSH concept]
- syndromic X-linked intellectual disability Shrimpton type [DO Concept]
Currated CISMeF NLP mapping
- X-linked intellectual disability, Shrimpton type [ORDO Disease]
- mental retardation, X-Linked, syndromic 9 [MeSH concept]
- mental retardation, X-Linked, syndromic 9 [MeSH Supplementary Concept]
DO Cross reference
- syndromic X-linked intellectual disability Shrimpton type [DO Concept]
HPO term(s)
- Intellectual disability [HPO term]
ORDO concept(s)
- X-linked intellectual disability, Shrimpton type [ORDO Disease]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- X-linked intellectual disability, Shrimpton type [ORDO Disease]
- mental retardation, X-Linked, syndromic 9 [MeSH Supplementary Concept]
- mental retardation, X-Linked, syndromic 9 [MeSH concept]

Keyword's position in hierarchy(ies) :

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