Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
Inherited vitreoretinopathy
rare
Identifiers
MONDO:0020246
Orphanet:98668
Part of
Hereditary neurological disease
Retinal disorder
Subtypes
All diseases
Rare only
Disease
Rare
Not rare
Subtypes
Vitreoretinal degeneration
MONDO:0020248
36
Congenital vitreoretinal dysplasia
MONDO:0020247
16
NDP-related vitreoretinopathy
MONDO:0700377
NDP
2
TSPAN12-related vitreoretinopathy
MONDO:0100484
TSPAN12
2
Vitreous detachment
MONDO:0007017
Projects
Including projects on subtypes.
Sign in to start a project
No projects yet.