Biopsy, Skin
Heterophile Antibody (Monospot) Test
Porphyria cutanea tarda
Mucopolysaccharidosis type II (Hunter Syndrome)
Hereditary Hemochromatosis (HFE) Mutation Assay
Immunoglobulin D (IgD)
Intrinsic Factor Blocking Antibody
Son of Sevenless Homolog 1 (SOS1) Gene Mutation Analysis
CACNA1A (calcium voltage-gated channel subunit alpha1 A) Gene Mutation Analysis
ANKK1/DRD2
LDS
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Spinocerebellar Ataxia, Ataxin 8 (ATXN8OS) Gene Mutation Analysis
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
Spinocerebellar Ataxia, Ataxin 8 (ATXN8OS) Gene Mutation Analysis
Medical Test
CPT
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Spinocerebellar Ataxia, Ataxin 8 (ATXN8OS) Gene Mutation Analysis
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