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familial progressive hyper- and hypopigmentation

Go to external page http://purl.obolibrary.org/obo/MONDO_0017239

Familial progressive hyper- and hypopigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by progressive, diffuse, partly blotchy, hyperpigmented lesions that are intermixed with multiple café-au-lait spots, hypopigmented maculae and lentigines and are located on the face, neck, trunk and limbs, as well as, frequently, the palms, soles and oral mucosa. Dispigmentation pattern can range from well isolated café-au-lait/hypopigmented patches on a background of normal-appearing skin to confetti-like or mottled appearance. [ Orphanet:280628 ]

Synonyms: FPHH

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C4706423 (MONDO:equivalentTo)
  • Orphanet:280628 (MONDO:equivalentTo)
  • MEDGEN:1643385 (MONDO:equivalentTo)
  • GARD:17298 (MONDO:GARD)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

exactMatch

http://linkedlifedata.com/resource/umls/id/C4706423

http://identifiers.org/medgen/1643385

http://www.orpha.net/ORDO/Orphanet_280628

id

MONDO:0017239