Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disorder of development or morphogenesis
/
Keratinization disease
/
Keratosis
/
Keratosis follicularis spinulosa decalvans
Keratosis follicularis spinulosa decalvans, autosomal dominant
rare
Identifiers
MONDO:0013018
OMIM:612843
Part of
Keratosis follicularis spinulosa decalvans
Also known as
KFSD
Projects
Sign in to start a project
No projects yet.