Ptosis, Hereditary Congenital 1 MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Ptosis, Hereditary Congenital 1
Unique ID: C566737
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566737
Registry Number: 0
Heading Mapped to: *Blepharoptosis
Frequency: 1
Note: aka PTOS1
Date of Entry: 2012/11/05

Ptosis, Hereditary Congenital 1 Preferred

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