MeSH Browser

MeSH Supplementary: Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant
Unique ID: C562625
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562625
Entry Term(s): Arthrochalasis Multiplex Congenita; EDS VII, Mutant Procollagen Type; EDS VIIA; EDS7A; Ehlers-Danlos Syndrome, Arthrochalasia Type
Registry Numbers: 0
Heading Mapped to: *Ehlers-Danlos Syndrome
Frequency: 3
Note: PROM mutation in COL1A1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

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