Ptosis, Hereditary Congenital 2 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Ptosis, Hereditary Congenital 2
Unique ID: C564553
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564553
Entry Term(s): Ptosis, X-Linked
Registry Numbers: 0
Heading Mapped to: *Blepharoptosis; *Genetic Diseases, X-Linked
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Ptosis, Hereditary Congenital 2 Preferred

page delivered in 0.004s