atkin syndrome

Preferred Label : atkin syndrome;

CISMeF synonym : mental retardation, X-linked nonspecific, type 1; mental retardation, X-linked, 21;

MeSH synonym : mental retardation X-linked atkin type; X-linked mental retardation syndrome, atkin type; Atkin-Flaitz syndrome; atkin flaitz patil smith syndrome; mental retardation X-linked, atkin type; MRX21;

MeSH hyponym : Mental Retardation, X-Linked 21;

Related MeSH term : Mental retardation, X-linked, nonspecific;

Détails

Origin ID

C538195;

UMLS CUI

C0796206;

Automatic exact mappings (from CISMeF team)
- IL1RAPL1 wt Allele [NCIt concept]
- non-syndromic X-linked intellectual disability [DO Concept]
Currated CISMeF NLP mapping
- Atkin-Flaitz syndrome [ORDO Disease]
- Atkin-flaitz syndrome [OMIM Phenotype]
- Intellectual developmental disorder, X-linked 21 [OMIM Phenotype]
- X-linked intellectual disability Atkin type (disorder) [SNOMED CT concept]
- non-syndromic X-linked intellectual disability 21 [DO Concept]
MeSH term(s) associated for indexing
- X-Linked Intellectual Disability [MeSH Descriptor]
Record concept(s)
- Atkin syndrome [MeSH concept]
- Mental retardation, X-linked nonspecific, type 1 [MeSH concept]
- Mental retardation, X-linked, 21 [MeSH concept]
See also inter- (CISMeF)
- IL1RAPL1 wt Allele [NCIt concept]
- Mental Retardation, X-linked 21/34 [NCIt concept]
- interleukin 1 receptor accessory protein like 1 [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atkin-Flaitz syndrome [ORDO Disease]
- Atkin-flaitz syndrome [OMIM Phenotype]
- Intellectual developmental disorder, X-linked 21 [OMIM Phenotype]
- X-linked intellectual disability Atkin type (disorder) [SNOMED CT concept]

Position du mot-clé dans l'(les) arborescence(s) :

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