Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness
rare
Identifiers
MONDO:0060496
OMIM:617519
Causal genes
SPTBN4
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDHND
Projects
Sign in to start a project
No projects yet.