Paroxysmal nocturnal hemoglobinuria
Myocarditis
WIPF1 Gene Mutation Analysis
Kallmann Syndrome, Xp22.3 Deletion, FISH
ACTH Stimulation Test (Cosyntropin)
Biopsy, Pericardial
Carnitine, Total, Serum/Plasma
Amyloid Beta Protein Ratio 1-42/1-40, Spinal Fluid
Neurofibromatosis Type 1 (NF1) Gene Mutation Analysis
Citrate Excretion for Kidney Stones, Random, Urine
LDS
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Friedreich's ataxia
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Medical Tests
ICD10
Additional ICD10
SNOMED
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Medical Tests
ICD10
Additional ICD10
SNOMED
Friedreich's ataxia
Disease
Additional ICD10
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Friedreich's ataxia
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