Congestive heart failure
Benign neoplasm, pancreas
Complement Component C4
Chronic gastritis
Idiopathic thrombocytopenic purpura
Malignant neoplasm, gallbladder
Acute myeloid leukemia (AML)
Postmeiotic Segregation Increased 2 (PMS2) Gene Mutation Analysis
Acute gastric ulcer
Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
LDS
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Uveal Melanoma, Chromosome 3 Monosomy, FISH, Tissue
All
Diseases
CPT
ICD10
Additional ICD10
All
Diseases
CPT
ICD10
Additional ICD10
Uveal Melanoma, Chromosome 3 Monosomy, FISH, Tissue
Medical Test
Diseases (1)
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