marshall syndrome

Preferred Label : marshall syndrome;

Details

Origin ID

D4-00711;

UMLS CUI

C0265235;

Automatic exact mappings (from CISMeF team)
- Marshall syndrome [ICD-11 More detail]
- Marshall syndrome [DO Concept]
- Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome [NCIt concept]
Currated CISMeF NLP mapping
- Marshall Syndrome [NCIt concept]
- Marshall syndrome [PASCAL descriptor]
- Marshall syndrome [Disease (Nov.)]
- Marshall syndrome [MeSH concept]
- Marshall syndrome [OMIM Phenotype]
- Marshall syndrome [ORDO Disease]
- Marshall syndrome (disorder) [SNOMED CT concept]
- marshall syndrome [MeSH Supplementary Concept]
Has phenotype(s) (HPO)
- Flattened nasal bridge [HPO term]
- Full lips [HPO term]
- Lens dislocation [HPO term]
- Mild platyspondyly [HPO term]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly affecting facial appearance [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Chondrodysplastic malformation syndrome [ORDO Disease]
- Ectodermal dysplasia syndrome [ORDO Disease]
- Rare disease with glaucoma as a major feature [ORDO Disease]
- Syndromic developmental defect of the eye [ORDO Disease]
- Syndromic myopia [ORDO Disease]
- Type 11 collagen-related bone disorder [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Marshall syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Marshall Syndrome [NCIt concept]
- Marshall syndrome [ORDO Disease]
- Marshall syndrome [MeSH concept]
- Marshall syndrome [OMIM Phenotype]
- Marshall syndrome [PASCAL descriptor]
- Marshall syndrome [DO Concept]
- Marshall syndrome (disorder) [SNOMED CT concept]
- marshall syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

Main resources

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