lymphedema, hereditary, II

Preferred Label : lymphedema, hereditary, II;

MeSH note : different from Meige Syndrome of idiopathic orofacial dyskinesia;

MeSH synonym : lymphedema, Late-Onset; meige lymphedema; lymphedema praecox; meige disease;

Détails

Origin ID

C562467;

UMLS CUI

C0238261;

Automatic exact mappings (from CISMeF team)
- Lymphedema praecox [ORDO Disease]
- Lymphedema praecox [MedDRA LLT]
- Lymphedema praecox (disorder) [SNOMED CT concept]
- Lymphoedema praecox [MedDRA LLT]
- Peripubertal primary lymphoedema [ICD-11 More detail]
- lymphedema praecox [SNOMED Notion]
Currated CISMeF NLP mapping
- Hereditary lymphedema type II (disorder) [SNOMED CT concept]
- Lymphatic malformation 5 [OMIM Phenotype]
- Meige disease [Disease (Nov.)]
- Meige disease [ORDO Disease]
- Trophoedema [MedDRA LLT]
- hereditary lymphedema II [DO Concept]
DO Cross reference
- hereditary lymphedema II [DO Concept]
MeSH term(s) associated for indexing
- lymphedema [MeSH Descriptor]
Record concept(s)
- lymphedema, hereditary, II [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphatic malformation 5 [OMIM Phenotype]
- Lymphedema praecox [MedDRA LLT]
- Lymphedema praecox [ORDO Disease]
- Lymphedema praecox (disorder) [SNOMED CT concept]
- Lymphoedema praecox [MedDRA LLT]
- lymphedema praecox [SNOMED Notion]

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