Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Autosomal genetic disease
/
Autosomal recessive disease
/
Ochoa syndrome
Urofacial syndrome type 1
rare
Identifiers
MONDO:0009368
OMIM:236730
Causal genes
HPSE2
Part of
Ochoa syndrome
Also known as
UFS1 · urofacial syndrome 1
Projects
Sign in to start a project
No projects yet.