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
/
Amelogenesis imperfecta
/
Hypocalcified amelogenesis imperfecta
Amelogenesis imperfecta type 3B
rare
Identifiers
MONDO:0021547
OMIM:617607
Part of
Hypocalcified amelogenesis imperfecta
Also known as
AI3B · amelogenesis imperfecta, type 3B · amelogenesis imperfecta, type IIIB
Projects
Sign in to start a project
No projects yet.