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
/
Cone-rod dystrophy and hearing loss
Cone-rod dystrophy and hearing loss 1
Identifiers
MONDO:0020778
OMIM:617236
Causal genes
CEP78
Part of
Cone-rod dystrophy and hearing loss
Also known as
CRDHL1
Projects
Sign in to start a project
No projects yet.