wittwer syndrome

Preferred Label : wittwer syndrome;

MeSH note : Prenatal and postnatal growth retardation, blindness, hearing loss, dysmorphic features, epilepsy, mental retardation and absence of speech;

Détails

Origin ID

C536737;

UMLS CUI

C0796202;

Automatic exact mappings (from CISMeF team)
- Wolf-hirschhorn syndrome [OMIM Phenotype]
Currated CISMeF NLP mapping
- Wittwer syndrome [OMIM Phenotype]
- X-linked intellectual disability, Wittwer type [ORDO Disease]
MeSH term(s) associated for indexing
- X-Linked Intellectual Disability [MeSH Descriptor]
- deaf-blind disorders [MeSH Descriptor]
- epilepsy [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
Record concept(s)
- Wittwer syndrome [MeSH concept]
See also (suggested by CISMeF)
- X-linked mental retardation type wittwer [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Wittwer syndrome [OMIM Phenotype]

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

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