Hyperparathyroidism, primary
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
TBP (TATA box binding protein) Gene Mutation Analysis
Chromosome Analysis, Hematologic Disorders, Bone Marrow
DNA Methylation Gene Panel for Barrett's Esophagus (EndoSign®)
Phenobarbital, Urine
Epilepsy
Lead/Creatinine Ratio, Random, Urine
Lactate Dehydrogenase (LDH), Serum
Henoch-Schönlein purpura
LDS
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Anemia, NOS
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Medical Tests
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SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Anemia, NOS
Disease
Medical Tests (56)
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