hyperpigmentation with or without hypopigmentation, familial progressive familial progressive hyper- and hypopigmentation https://www.malacards.org/card/familial_progressive_hyper_and_hypopigmentation FPHH MONDO:0017239 MEDGEN:1643385 icd11.foundation:1229773662 Orphanet:280628 UMLS:C4706423 GARD:0017298 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.