MeSH Browser

MeSH Supplementary: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Unique ID: C562424
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562424
Entry Term(s): Ehlers-Danlos Syndrome, Friedman-Harrod Type
Registry Numbers: 0
Heading Mapped to: *Ehlers-Danlos Syndrome
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified MeSH Supplementary Concept Data 2025