ptosis, hereditary congenital 2

Preferred Label : ptosis, hereditary congenital 2;

MeSH synonym : ptosis, X-Linked;

Origin ID

C564553;

UMLS CUI

C1846128;

Currated CISMeF NLP mapping
- Ptosis, hereditary congenital 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- blepharoptosis [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
Record concept(s)
- ptosis, hereditary congenital 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ptosis, hereditary congenital 2 [OMIM Phenotype]