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Fabry disease

MONDO:0010526

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

Also known as: Alpha-galactosidase A deficiency, Anderson-Fabry disease, FD, Fabry disease, Fabry's disease, Fd, angiokeratoma corporis diffusum, diffuse angiokeratoma

96 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inherited lipid metabolism disorder (165) Inborn errors of metabolism (42) Lysosomal storage disease (33) Human disease (14) Developmental defect during embryogenesis (7) Sphingolipidosis (4) Disease of genetic or genomic mechanism (2)

Trials to join now! 39 Not yet recruiting 8 Not yet finished but already full! 15 Completed 33 Terminated 1

Fabry disease sperm study halted early

Knowledge-focused Terminated

This study aimed to find out how common sperm problems are in men with Fabry disease. Researchers planned to check sperm samples from 22 men aged 18 to 65. The study was stopped early, so results are limited.

Phase: NA • Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:00 UTC

Fabry disease

Broader categories

Fabry disease sperm study halted early