Additional Disease Briefs

familial partial lipodystrophy, Kobberling type

Also known as: FPLD1, familial partial lipodystrophy type 1, familial partial lipodystrophy type Köbberling, familial partial lipodystrophy, Köbberling type, lipodystrophy, familial partial, Kobberling type, lipodystrophy, familial partial, type 1

familial porphyria cutanea tarda

Also known as: PCT, PCT, 'familial' type, PCT, type 2, Urod deficiency, hereditary porphyria cutanea tarda, porphyria cutanea tarda, porphyria cutanea tarda type II, porphyria cutanea tarda, susceptibility to, porphyria cutanea tarda, type 2, porphyria, Hepatocutaneous type, porphyria, hepatoerythropoietic, uroporphyrinogen decarboxylase deficiency

familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis

Also known as: FHHNC, Michellis-Castrillo syndrome

familial primary hypomagnesemia with hypocalcuria

familial primary pulmonary hypoplasia

Also known as: lung agenesis, primary pulmonary hypoplasia, pulmonary hypoplasia, primary

familial progressive hyper- and hypopigmentation

Also known as: FPHH

familial progressive hyperpigmentation

Also known as: FPH1, Fph, hyperpigmentation, familial progressive, 1, melanosis diffusa congenita, melanosis universalis hereditaria, universal melanosis

familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome

Also known as: RDICC, retinal dystrophy and iris coloboma with or without cataract, retinal dystrophy and iris coloboma with or without congenital cataract

familial prostate carcinoma

familial pseudohyperkalemia

Also known as: PSHK2, cryohydrocytosis, mild, pseudohyperkalemia Chiswick, pseudohyperkalemia East London, pseudohyperkalemia Falkirk, pseudohyperkalemia Lille, pseudohyperkalemia, familial, 2, due to red cell leak