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Differential Diagnosis For Patient/Fabrys disease


List of current finding(s):

Metabolic, Storage Disorders
Fabrys disease/Angiokeratatosis (trihexose ceramide)
Hereditary, Familial, Genetic Disorders
Fabry disease crisis/syndrome
Anatomic, Foreign Body, Structural Disorders
Mitral valve insufficiency
Arteriosclerotic, Vascular, Venous Disorders
Myocardial infarction, acute
Stroke syndrome
Cardiomyopathy, ischemic
Reference to Organ System
Renal Failure Chronic
ALPHA GALACTOSIDASE A DEFIC DIS, alpha Galactosidase A Deficiency Disease, alpha galactosidase deficiency, Alpha-galactosidase A defic, Alpha-galactosidase A deficiency, alpha-Galactosidase A Deficiency Disease, alpha-Galactosidase-A deficiency, Anderson Fabry Disease, Anderson-Fabry, Anderson-Fabry disease, Angiokeratoma corporis diffusm, Angiokeratoma Corporis Diffusum, Angiokeratoma corporis diffusum universale, Cardiovasorenal syndrome, Ceramide lactoside lipidosis, Ceramide trihexosidase defic, Ceramide trihexosidase deficiency, CERAMIDE TRIHEXOSIDE LIPOIDOSIS (FABRYS DISEASE), CERAMIDE TRIHEXOSIDE LIPOIDOSIS FABRYS DISEASE, ceramide trihexosidosis, corporis diffusum angiokeratoma, Deficiency of alpha-galactosidase, Deficiency of alpha-galactosidase (disorder), Deficiency of melibiase, Disease Fabry, Fabry, FABRY DIS, Fabry disease, Fabrys Disease, Fabry's disease, Fabry's disease (disorder), GLA deficiency, Hereditary dystopic lipidosis, Lactosyl ceramidosis, Patient, Ruiter-Pompen syndrome, Sweeley-Klionsky disease, Thesaurismosis hereditaria, Thesaurismosis lipoidica, Trihexosidase deficiency disease
External Links Related to Patient/Fabrys disease
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)