Glycogen storage disease type II (Pompe disease)
Williams Syndrome, 7q11.23 Deletion, FISH, CV
Beta-2 Glycoprotein 1 Antibody, IgM
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Lead, Blood
PAX2, Immunohistochemistry, Tissue
Ehrlichia Antibody, Western Blot
Hemoglobin A1c
Cytomegalovirus (CMV) Antibody, IgG
Neurotrophic Receptor Tyrosine Kinase 1 (NTRK1) Gene Mutation Analysis (Translocation)
LDS
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Hepatic coma
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Medical Tests
ICD10
Additional ICD10
SNOMED
Hepatic coma
Disease
Medical Tests (28)
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Hepatic coma
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ICD10
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Hepatic coma
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Additional ICD10
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Hepatic coma
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SNOMED
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Hepatic coma
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