You are using an outdated browser. Please upgrade your browser to improve your experience.
keratosis follicularis spinulosa decalvans
Disease Summary
Associated Targets (3)
Tbio
3
Mondo Description Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterized by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma.
Download Data for keratosis follicularis spinulosa decalvans
data still loading...
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DC:0000550
GARD:0006829
Orphanet:2340
SCTID:238626006
MONDO:0000136
High level summary of knowledge for a disease, including descriptions and datasource references.