Marshall syndrome

Preferred Label : Marshall syndrome;

ICD-11 definition : Marshall syndrome is a multisystem autosomal dominant disease characterized by ocular abnormalities, sensorineural hearing loss, craniofacial anomalies and anhidrotic ectodermal dysplasia.;

Détails

Origin ID

1401051186;

Automatic exact mappings (from CISMeF team)
- Marshall Syndrome [NCIt concept]
- Marshall syndrome [PASCAL descriptor]
- Marshall syndrome [ORDO Disease]
- Marshall syndrome [MeSH concept]
- Marshall syndrome [OMIM Phenotype]
- Marshall syndrome [DO Concept]
- Marshall syndrome (disorder) [SNOMED CT concept]
- Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome [NCIt concept]
- marshall syndrome [MeSH Supplementary Concept]
- marshall syndrome [SNOMED Notion]

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

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