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familial generalized lentiginosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0007891

Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa. [ Orphanet:231040 ]

Synonyms: familial multiple lentigines syndrome without systemic involvement familial lentigines profusa

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:765195000 (MONDO:equivalentTo)
  • MEDGEN:486897 (MONDO:equivalentTo)
  • GARD:17158 (MONDO:GARD)
  • OMIM:151001 (Orphanet:231040/e)
  • Orphanet:231040 (OMIM:151001)
  • UMLS:C3492944 (MONDO:equivalentTo)
  • MESH:C573023 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

exactMatch

https://omim.org/entry/151001

http://identifiers.org/mesh/C573023

http://identifiers.org/snomedct/765195000

http://linkedlifedata.com/resource/umls/id/C3492944

http://www.orpha.net/ORDO/Orphanet_231040

http://identifiers.org/medgen/486897

has related synonym

lentiginosis profusa

lentiginosis, generalized

lentiginosis, inherited patterned

lentiginosis, generalised

lentiginosis, diffuse

id

MONDO:0007891

Term relations