5C56.01Ангилал

Fabry disease

Тодорхойлолт

Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterised by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

Индексийн нэр томьёо Index terms · 8

Fabry diseaseAnderson-Fabry diseaseCeramide trihexosidase deficiencyAlpha-galactosidase A deficiencyFabry disease X-linkedX-linked dominant Fabry diseaseX-linked recessive Fabry diseaseAngiokeratoma corporis diffusum

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