MeSH Browser

MeSH Supplementary: Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction
Unique ID: C563394
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563394
Registry Numbers: 0
Heading Mapped to: *Ectodermal Dysplasia; *Myopia; *Vision Disorders; *Nystagmus, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction MeSH Supplementary Concept Data 2025