Biopsy, Gallbladder (Cholecystectomy)
Nexilin-like Protein (NEXN) Gene Mutation Analysis
Biopsy, Adrenal
Alanine Aminotransferase (ALT)
Fungal Culture, Body Fluid
Fragile X syndrome
Bartonella Antibody, IgG and IgM, Serum
Oligoclonal Bands, CSF
22q11.2 deletion syndrome
PLOD1 Gene Mutation Analysis
LDS
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hypochondroplasia
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Medical Tests
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Additional ICD10
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Additional ICD10
SNOMED
hypochondroplasia
Disease
Additional ICD10
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hypochondroplasia
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