Category:Fabry disease

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Radiology: Magnetic resonance | Anatomical pathology: Histopathology |
Deutsch: Fabry-Anderson-Krankheit.
<nowiki>enfermedad de Fabry; Fabryjeva bolezen; maladie de Fabry; Фабри чире; Fabry tõbi; Fabri kasalligi; Fabry disease; Fabryn tauti; Болезнь Фабри; Хвороба Фабрі; Morbus Fabry; doença de Fabry; malattia di Fabry; Ֆաբրիի հիվանդություն; 法布瑞氏症; Фабријева болест; Fabry hastalığı; فیبری بیماری; doença de Fabry; malaltia de Fabry; Anderson-Fabrys sjukdom; Choroba Fabry'ego; מחלת פברי; 法布瑞氏症; ziekte van Fabry; 法布雷病; ファブリー病; 파브리병; Doenza de Fabry; مرض فابري; Фабриева болест; بیماری فابری; malattia umana; Maladie génétique; rzadka, genetycznie uwarunkowana choroba; лізосомні хвороби накопичення; erfelijke ziekte; редкое генетически детерминированное заболевание из группы лизосомных болезней накопления; seltene angeborene Stoffwechselkrankheit; perinnöllinen entsyyminpuutostauti; rare human genetic lysosomal storage disorder; خلل وراثي نادر سببه عيب في إحدى مورّثات الجسم; tipo de doença; doenza xenética rara; malaltia d'Anderson-Fabry; 法布里病; Fabry's disease; Anderson-Fabry disease; angiokeratoma corporis diffusum; alpha-galactosidase A deficiency; Fabry's disease (disorder); alpha galactosidase deficiency; deficiency of melibiase; Hereditary Dystopic Lipidosis; Fabry Disease, Cardiac Variant; Ceramide Trihexosidase Deficiency; Diffuse angiokeratoma; FD; Gla Deficiency; FABRY DISEASE; Fabry's angiokeratosis; α-半乳糖苷酶缺乏症; lipidosi glicolipidica; malattia di Anderson-Fabry; sindrome di Anderson; morbo di Ruiter-Pompen; sindrome di Ruiter-Pompen-Wyers; malattia di Sweeley-Klionsky; angiocheratoma corporis diffusum; deficit di alfa-galattosidasi; porpora emorragica nodulare; angiocheratoma diffuso</nowiki>
Fabry disease 
rare human genetic lysosomal storage disorder
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Instance of
Subclass of
  • sphingolipidosis
  • developmental anomaly of metabolic origin
  • genetic skin vascular disorder
  • rare genetic epilepsy
  • syndromic dyslipidemia
  • vascular skin disease
  • hypertrophic cardiomyopathy
  • sphingolipidosis with epilepsy
  • syndromic lymphedema
  • nephropathy secondary to a storage or other metabolic disease
  • cataract associated with a metabolic disease
  • metabolic disease with corneal opacity
  • lysosomal disease with restrictive cardiomyopathy
  • lysosomal disease with hypertrophic cardiomyopathy
  • rare hereditary metabolic disease with peripheral neuropathy
  • syndrome associated with hypertrophic cardiomyopathy
  • disease
Named after
Authority file
Wikidata Q615645
GND ID: 4153455-4
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Subcategories

This category has the following 4 subcategories, out of 4 total.

 

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Media in category "Fabry disease"

The following 35 files are in this category, out of 35 total.

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