Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
Psychosine, Blood
Temazepam, Urine
Hepatitis B Virus (HBV) by Molecular Method, Quantitative (Viral Load)
Glycogen storage disease type I (von Gierke disease)
Lactate Dehydrogenase (LDH), Body Fluid
Direct Antiglobulin (Direct Coombs) Test
Neuroendocrine Neoplasms (Carcinoid Tumors)
Electrophoresis, Protein, 24 Hour, Urine
Follicular Lymphoma, bcl-2/JH t(14;18), Real-time PCR, Tissue
LDS
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Disease
Additional ICD10
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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