Gamuts

Fabry disease

Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, and skin. Fabry disease is one of a group of conditions known as lysosomal storage diseases. [Source: Wikipedia ]

OrphaNet reference
Fabry disease 
May Cause
Anhidrosis
Avascular necrosis
Bilateral large kidneys
Cardiomegaly
Cardiomyopathy
Congenital cardiomyopathy
Congenital heart disease
Congenitally limited joint mobility
Epiphyseal necrosis
Fragmented or irregular femoral head
Gastrointestinal dysfunction
Hypohidrosis
Limited joint mobility
Myocardial infarction
Nephropathy
Systemic hypertension
OrphaNet reference
Fabry disease 
May Cause
Anhidrosis
Avascular necrosis
Bilateral large kidneys
Cardiomegaly
Cardiomyopathy
Congenital cardiomyopathy
Congenital heart disease
Congenitally limited joint mobility
Epiphyseal necrosis
Fragmented or irregular femoral head
Gastrointestinal dysfunction
Hypohidrosis
Limited joint mobility
Myocardial infarction
Nephropathy
Systemic hypertension


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