Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Syndromic disease
Lopes-Maciel-Rodan syndrome
rare
Identifiers
MONDO:0054573
OMIM:617435
Causal genes
HTT
Part of
Hereditary disease
Syndromic disease
Also known as
LOMARS
Projects
Sign in to start a project
No projects yet.