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
Dilution, pigmentary
rare
Identifiers
MONDO:0007459
OMIM:126070
Part of
Hereditary disease
Also known as
hypomelanotic disorder
Projects
Sign in to start a project
No projects yet.