Klippel-Trenaunay Syndrome
TERC Gene Mutation Analysis
Hematolymphoid Neoplasm Gene Mutation Panel, NGS
Brucella Nucleic Acid Detection by PCR
Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
Ehlers-Danlos Syndrome Gene Mutation Panel, NGS
Hepatic coma
Biopsy, Skin, Direct Immunofluorescence
Chromosome Breakage Study, Chorionic Villi
Proteinase 3 Antibody, IgG
LDS
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Fabry (Anderson) disease
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Medical Tests
ICD10
Additional ICD10
SNOMED
All
Medical Tests
ICD10
Additional ICD10
SNOMED
Fabry (Anderson) disease
Disease
Medical Tests (20)
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Fabry (Anderson) disease
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ICD10
Access to
Fabry (Anderson) disease
is restricted.
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Additional ICD10
Access to
Fabry (Anderson) disease
is restricted.
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SNOMED
Access to
Fabry (Anderson) disease
is restricted.
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