A rare mitochondrial disease with marked clinical variability typically and characteristics of encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Add

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syndroom van doofheid, encefaloneuropathie, obesitas en klepinsufficiëntie

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Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

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spinocerebellaire ataxie type 38

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Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin:disease | haemoglobinuria | Haemolytic anaemia:cold type (secondary)(symptomatic) | warm type (secondary)(symptomatic)

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Enteroviral lymphonodular pharyngitis Foot-and-mouth disease Tanapox virus disease Yaba pox virus disease

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lymfonodulaire faryngitis door enterovirus | Tana-pokken | voet- en mondziekte | Yaba-pokken

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Anderen hebben gezocht naar : basedow's disease cardiac glycogenosis disease andersen flajani's disease forbes gsd-ii graves disease graves's disease haemolytic anaemia cold type liver phosphorylase deficiency march's disease mcardle parry disease parry's disease pompe disease stokes's disease acid maltase deficiency blue disease blue ear disease blue-ear disease of pigs disease exophthalmic goiter glycogen storage disease type ii glycogenosis type ii haemoglobinuria human disease illness mysterious pig disease mysterious swine disease mystery pig disease new pig disease porcine epidemical abortion porcine reproductive and respiratory syndrome purple ears disease thyrotoxicosis von gierke warm type Pompe disease

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'Pompe disease' ->

Date index: 2021-07-23