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Fabry disease
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Genetic Markers
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GLA
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
raffinose alpha-galactosidase activity
Glycoside hydrolase family 27/36, conserved site
Alpha galactosidase A, C-terminal beta-sandwich domain
Glycoside hydrolase, family 27
MODULE_492
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Mouse Phenotypes - Kidney diseases
OMIM - Congenital disorder
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Most Relevant Literature
Hemoporfin-mediated photodynamic therapy for angiokeratoma corporis diffusum: A case report.
Pain therapy for Fabry's disease].
Angiokeratoma corporis diffusum with severe acroparesthesia, an endothelial abnormality, and inconsp…
Diagnosing lysosomal storage disorders: Fabry disease.
Fabry disease: a review of ophthalmic and systemic manifestations.
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Canadian Fabry Disease Initiative (CFDI) National Registry
Establishment of Biomarkers for Fabry Disease
Antiproteinuric Agents and Fabry Disease
Fabry Disease in Cerebrovascular Disease
Study of the Spermatic Characteristics of Patients With Fabry Disease
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