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keratosis pilaris atrophicans
Disease Summary
Associated Targets (3)
Tbio
3
Mondo Description An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair.
Uniprot Description A group of rare genodermatoses characterized by keratotic follicular papules, variable degrees of inflammation, and secondary atrophic scarring. Most cases are associated with an atopic diathesis and keratosis pilaris on the extensor extremities. KPA is comprised of three distinct clinical subtypes: keratosis pilaris atrophicans faciei, atrophoderma vermiculatum, and keratosis follicularis spinulosa decalvans. Affected individuals may present with features overlapping the 3 subtypes.
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.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0001042
MESH:C537412
OMIM:604093
Orphanet:498
SCTID:400059005
MONDO:0018855
High level summary of knowledge for a disease, including descriptions and datasource references.