aldred syndrome

Preferred Label : aldred syndrome;

MeSH synonym : X-linked mental handicap-retinitis pigmentosa syndrome; nonspecific mental retardation associated with retinitis pigmentosa;

Détails

Origin ID

C537046;

UMLS CUI

C0795873;

Automatic exact mappings (from CISMeF team)
- Chromosome Xp11.3 microdeletion syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- X-linked intellectual disability-retinitis pigmentosa syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- X-Linked Intellectual Disability [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Aldred syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome Xp11.3 microdeletion syndrome (disorder) [SNOMED CT concept]
- X-linked intellectual disability-retinitis pigmentosa syndrome [ORDO Disease]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients