Oliver syndrome

Preferred Label : Oliver syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Postaxial polydactyly and mental retardation;

Inheritance : Autosomal recessive;

Prefixed ID : 258200;

Details

Origin ID

258200;

UMLS CUI

C1850320;

Automatic exact mappings (from CISMeF team)
- Oliver syndrome [ICD-11 More detail]
- Postaxial polydactyly and intellectual disability syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Oliver syndrome [ORDO Disease]
- oliver syndrome [MeSH concept]
- oliver syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Intellectual disability [HPO term]
- Postaxial hand polydactyly [HPO term]
ORDO concept(s)
- Oliver syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Oliver syndrome [ORDO Disease]
- Postaxial polydactyly and intellectual disability syndrome (disorder) [SNOMED CT concept]
- oliver syndrome [MeSH Supplementary Concept]
- oliver syndrome [MeSH concept]

Keyword's position in hierarchy(ies) :

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