Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Methaqualone, Urine
Coagulation Factor V Activity Assay, Plasma
HER2/neu (ERBB2), IHC, Semi-Quantitative, Other Tissue
Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
Ferritin
Bone Morphogenetic Protein Receptor Type II (BMPR2) Gene Mutation Analysis
ATN1 (Atrophin 1) Gene Mutation Analysis
CD4/CD8 Lymphocyte Ratio, Bronchoalvolar lavage
LDS
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LDS
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Diseases
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Multiple endocrine neoplasia, type II
All
Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Multiple endocrine neoplasia, type II
Disease
Additional ICD10
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Multiple endocrine neoplasia, type II
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