mental retardation, X-linked, syndromic 5

Preferred Label : mental retardation, X-linked, syndromic 5;

MeSH synonym : mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures; pettigrew syndrome; Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures;

Details

Origin ID

C535773;

UMLS CUI

C0796254;

Currated CISMeF NLP mapping
- Pettigrew Syndrome [NCIt concept]
- Pettigrew syndrome [OMIM Phenotype]
- X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) [SNOMED CT concept]
- X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome [ORDO Disease]
- syndromic X-linked intellectual disability 5 [DO Concept]
DO Cross reference
- syndromic X-linked intellectual disability 5 [DO Concept]
MeSH term(s) associated for indexing
- Dandy-Walker syndrome [MeSH Descriptor]
- basal ganglia diseases [MeSH Descriptor]
- mental retardation, X-Linked [MeSH Descriptor]
- seizures [MeSH Descriptor]
Record concept(s)
- Mental retardation, X-linked, syndromic 5 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pettigrew Syndrome [NCIt concept]
- Pettigrew syndrome [OMIM Phenotype]
- X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) [SNOMED CT concept]
- X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome [ORDO Disease]
- syndromic X-linked intellectual disability 5 [DO Concept]

Keyword's position in hierarchy(ies) :

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