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
Brachydactyly, type A2, with microcephaly
Identifiers
MONDO:0008883
OMIM:211369
Part of
Hereditary disease
Projects
Sign in to start a project
No projects yet.