Additional Disease Briefs

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FLOTCH syndrome

Also known as: familial occurrence of total leukonychia, trichilemmal cysts and ciliary dystrophy with dominant autosomal heredity, leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome


FLVCR1-related retinopathy with or without ataxia

Also known as: AXPC1, FLVCR1 retinopathy with or without ataxia, PCARP, ataxia, posterior column, with retinitis pigmentosa, autosomal recessive posterior column ataxia and retinitis pigmentosa, posterior column ataxia with retinitis pigmentosa, posterior column ataxia-retinitis pigmentosa syndrome


focal acral hyperkeratosis

Also known as: PPKP3 without elastoidosis, PPPK3 without elastoidosis, punctate palmoplantar hyperkeratosis type 3 without elastoidosis, punctate palmoplantar keratoderma type 3 without elastoidosis




focal facial dermal dysplasia type I

Also known as: Brauer syndrome, FFDD type I, FFDD, type 1, FFDD1, bitemporal aplasia cutis congenita, focal facial dermal dysplasia 1, Brauer type, focal facial dermal dysplasia type 1, hereditary symmetrical aplastic nevi of temples


focal facial dermal dysplasia type III

Also known as: FFDD type 2, FFDD type III, FFDD3, Setleis syndrome, bitemporal forceps Marks syndrome, bitemporal forceps marks syndrome, facial ectodermal dysplasia, focal Facial dermal dysplasia, type II, focal Facial dermal dysplasia, type II, formerly, focal facial dermal dysplasia 3, Setleis type, focal facial dermal dysplasia type 2, focal facial dermal dysplasia type III