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keratosis pilaris atrophicans

^ http://purl.obolibrary.org/obo/MONDO_0018855

An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair. [ https://www.dermnetnz.org/topics/keratosis-pilaris/ ]

Term info

database cross reference
  • SCTID:400059005 (MONDO:equivalentTo)
  • Orphanet:498 (MONDO:equivalentTo)
  • DOID:0080751 (MONDO:equivalentTo)
  • OMIM:604093 (MONDO:equivalentTo)
  • GARD:0001042 (MONDO:equivalentTo)
  • ICD9:757.39 (MONDO:relatedTo)
  • MESH:C537412 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, ordo_group_of_disorders

abbreviation
KPA [ OMIM:604093 ]

definition

An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair.

exactMatch

http://purl.obolibrary.org/obo/DOID_0080751, https://omim.org/entry/604093, http://purl.obolibrary.org/obo/Orphanet_498, http://identifiers.org/mesh/C537412, http://identifiers.org/snomedct/400059005

has exact synonym

keratosis pilaris atrophicans

has related synonym

keratosis pilaris atrophicans facies, Atrophodermia reticulata symmetrica faciei, ulerythema ophryogenes with multiple congenital anomalies, Atrophodermia vermiculata, Atrophodermia reticulata, ulerythema ophryogenes, keratosis pilaris, amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2, burnett Schwartz Berberian syndrome, honeycomb atrophy, ulerythema ophryogenesis, folliculitis ulerythematosa, folliculitis ulerythematosa reticulata, KPA

id

MONDO:0018855

seeAlso

https://rarediseases.info.nih.gov/diseases/1042/burnett-schwartz-berberian-syndrome

Term relations