Apolipoprotein B (APOB) Mutation Detection
Benign neoplasm of esophagus
Carotene, Total, Serum
TGFBI Gene Mutation Analysis
Idiopathic and Hereditary Pancreatitis
BCR-ABL Translocation by RT-PCR, Quantitative, Bone Marrow
Atrial fibrillation
HOXB13 (G84E) Gene Mutation Analysis
Occult Blood, Fecal by Immunoassay
Autoinflammation & PLCG2-associated Antibody Deficiency and Immune Dysregulation (APLAID)
LDS
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Finnish lactic acidosis with hepatic hemosiderosis (GRACILE Syndrome)
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Finnish lactic acidosis with hepatic hemosiderosis (GRACILE Syndrome)
Disease
Additional ICD10
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Finnish lactic acidosis with hepatic hemosiderosis (GRACILE Syndrome)
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