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familial multiple fibrofolliculoma

^ http://purl.obolibrary.org/obo/MONDO_0018070

Familial multiple fibrofolliculoma is a genodermatosis characterised by the presence of multiple hamartomas of the hair follicle. It has been described in one family so far. [ Orphanet:338 ]

Term info

database cross reference
  • Orphanet:338 (MONDO:equivalentTo)
  • UMLS:C4509837 (MONDO:equivalentObsolete)
  • SCTID:723361006 (MONDO:equivalentTo)
  • UMLS:CN204388 (MONDO:equivalentTo)
  • GARD:0003831 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

definition

Familial multiple fibrofolliculoma is a genodermatosis characterised by the presence of multiple hamartomas of the hair follicle. It has been described in one family so far.

exactMatch

http://identifiers.org/snomedct/723361006, http://linkedlifedata.com/resource/umls/id/CN204388, http://purl.obolibrary.org/obo/Orphanet_338

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019300

has related synonym

multiple fibrofolliculoma familial

id

MONDO:0018070

seeAlso

https://rarediseases.info.nih.gov/diseases/3831/multiple-fibrofolliculoma-familial

Term relations

Subclass of: