Yellow Nail Syndrome

Preferred Label : Yellow Nail Syndrome;

NCIt definition : A rare syndrome characterized by the presence of thickened yellow nails, lymphedema, and respiratory abnormalities, including pleural effusion, bronchiectasis, chronic sinusitis, and persistent cough. Some cases are associated with mutations in the FOXC2 gene.;

Details

Origin ID

C85238;

UMLS CUI

C0221348;

Currated CISMeF NLP mapping
- Hereditary lymphedema and yellow nails (disorder) [SNOMED CT concept]
- YELLOW NAIL SYNDROME [WHO-ART Preferred Term]
- Yellow nail syndrome [PASCAL descriptor]
- Yellow nail syndrome [ICD-10 Sub-category]
- Yellow nail syndrome [ICD-11 Subcategory]
- Yellow nail syndrome [ICD-10 Sub-category (who)]
- Yellow nail syndrome [MedDRA Preferred Term]
- Yellow nail syndrome [OMIM Phenotype]
- Yellow nail syndrome [ORDO Disease]
- Yellow nails (finding) [SNOMED CT concept]
- yellow nail syndrome [DO Concept]
- yellow nail syndrome [MeSH Descriptor]
- yellow nail syndrome [MeSH concept]
- yellow nail syndrome [SNOMED Notion]
DO Cross reference
- yellow nail syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary lymphedema and yellow nails (disorder) [SNOMED CT concept]
- YELLOW NAIL SYNDROME [WHO-ART Preferred Term]
- Yellow nail syndrome [OMIM Phenotype]
- Yellow nail syndrome [ICD-10 Sub-category]
- Yellow nail syndrome [ORDO Disease]
- Yellow nail syndrome [ICD-10 Sub-category (who)]
- Yellow nail syndrome [MedDRA Preferred Term]
- yellow nail syndrome [DO Concept]
- yellow nail syndrome [MeSH concept]
- yellow nail syndrome [MeSH Descriptor]
- yellow nail syndrome [SNOMED Notion]
Validated automatic mappings to BTNT
- Yellow nails [HPO term]
disease_has_finding
- Rare Lesion [NCIt concept]
related_to_genetic_biomarker
- FOXC2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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