Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Arthrogryposis multiplex congenita
Arthrogryposis multiplex congenita 6
rare
Identifiers
MONDO:0030281
OMIM:619334
Causal genes
NEB
Part of
Arthrogryposis multiplex congenita
Also known as
AMC6
Projects
Sign in to start a project
No projects yet.