Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Autosomal genetic disease
/
Autosomal dominant disease
Arthrogryposis, distal, type 2B2
rare
Identifiers
MONDO:0032750
OMIM:618435
Causal genes
TNNT3
Part of
Sheldon-hall syndrome
Autosomal dominant disease
Also known as
DA2B2
Projects
Sign in to start a project
No projects yet.