Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [Supplementary Concept]
PROM mutation in COL1A1
Date introduced: November 5, 2012
MeSH Unique ID: C562625
Heading Mapped to:
Entry Terms:
- Arthrochalasis Multiplex Congenita
- EDS VII, Mutant Procollagen Type
- EDS VIIA
- EDS7A
- Ehlers-Danlos Syndrome, Arthrochalasia Type