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radioulnar synostosis
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Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
HOXA11
MECOM
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
IZADPANAH_STEM_CELL_ADIPOSE_VS_BONE_UP
HP1SITEFACTOR_Q6
Domain of unknown function DUF3528, homeobox protein, eukaryotic
PTF1BETA_Q6
FOXO4_01
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Mouse Phenotypes - Congenital abnormality
OMIM - Radioulnar synostosis
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report.
Congenital Radioulnar Synostosis.
A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis.
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variant…
Derotational Osteotomy and Plate Fixation of the Radius and Ulna for the Treatment of Congenital Pro…
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There were no clinical trials for radioulnar synostosis
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