rombo syndrome

Preferred Label : rombo syndrome;

MeSH note : Vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis;

Details

Origin ID

C535870;

UMLS CUI

C1867147;

CISMeF manual mappings
- Rombo syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Rombo syndrome [PASCAL descriptor]
- Rombo syndrome [OMIM Phenotype]
- Rombo syndrome [ORDO Disease]
Has phenotype(s) (HPO)
- absent/abnormal eyelashes and eyebrows [HPO term]
MeSH term(s) associated for indexing
- carcinoma, basal cell [MeSH Descriptor]
- cyanosis [MeSH Descriptor]
- facial dermatoses [MeSH Descriptor]
- hypotrichosis [MeSH Descriptor]
- skin neoplasms [MeSH Descriptor]
ORDO relation(s)
- Rombo syndrome [ORDO Disease]
Record concept(s)
- Rombo syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Rombo syndrome [ORDO Disease]
- Rombo syndrome [OMIM Phenotype]
- Rombo syndrome [PASCAL descriptor]
- Rombo syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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