Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Syndromic disease
/
Fanconi renotubular syndrome
/
Inherited Fanconi renotubular syndrome
Fanconi renotubular syndrome 5
rare
Identifiers
MONDO:0030056
OMIM:618913
Causal genes
NDUFAF6
Part of
Inherited Fanconi renotubular syndrome
Also known as
Fanconi Renotubular Syndrome, Acadian Variant · FRTS5
Projects
Sign in to start a project
No projects yet.