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autosomal dominant hereditary disorder
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
YY1
APC
RAF1
FGFR2
PTPN11
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
regulation of nitrogen compound metabolic process
heterocyclic compound binding
organic cyclic compound binding
heterocycle metabolic process
organic cyclic compound metabolic process
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Curated Studies
Most Correlated Studies
Facioscapulohumeral muscular dystrophy expression profiling of bicepts and deltoid muscles
Skeletal muscle myoblasts and myotubes cultured from facioscapulohumeral dystrophy patients
Rhabdomyosarcoma RD cells ectopically expressing double homeobox 4 (DUX4)
Myoblast C2C12 cells ectopically expressing human double homeobox 4 (DUX4)
Outgrowth endothelial cells from Loeys-Dietz syndrome patients
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Literature
Most Relevant Literature
Calculating risk changes after negative mutation test outcomes for autosomal dominant hereditary lat…
Parasitic myomas after laparoscopic-assisted myomectomy in multiple endocrine neoplasia type 1.
A novel genetic disorder of Lynch syndrome - EPCAM gene deletion].
Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochon…
Villous papillary thyroid carcinoma: a variant associated with marfan syndrome.
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Clinical Trials
Most Relevant Clinical Trials
Biomarkers in Autosomal Dominant Cerebellar Ataxia
Biomarker for Hereditary AngioEdema Disease
Diet as a Potential Treatment for Autosomal Dominant Polycystic Kidney Disease
Epidemiology of Non-syndromic Dominant Deafness
Hereditary Angioedema Kininogen Assay
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