eccrine syringofibroadenomatosis with eyelid abnormalities

Preferred Label : eccrine syringofibroadenomatosis with eyelid abnormalities;

Origin ID

C566347;

UMLS CUI

C1863618;

Currated CISMeF NLP mapping
- Eccrine syringofibroadenomatosis with eyelid abnormalities [OMIM Phenotype]
MeSH term(s) associated for indexing
- eccrine glands [MeSH Descriptor]
- eyelid diseases [MeSH Descriptor]
- eyelids [MeSH Descriptor]
- fibroadenoma [MeSH Descriptor]
Record concept(s)
- eccrine syringofibroadenomatosis with eyelid abnormalities [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Eccrine syringofibroadenomatosis with eyelid abnormalities [OMIM Phenotype]