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camptodactyly
(phenotype)
Summary
General Info
Genetic Markers
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Most Correlated SNPs
PRG4
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
Somatomedin B, chordata
Somatomedin B-like domain superfamily
KONG_E2F1_TARGETS
Somatomedin B domain
Hemopexin, conserved site
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Curated Studies
Most Correlated Studies
OMIM - Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
OMIM - Camptosynpolydactyly
OMIM - CATSHL syndrome
Mouse Phenotypes - Congenital disorder
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Camptodactyly: a 10-year series.
Camptodactyly].
A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericardit…
Peters anomaly with post axial polydactyly, bilateral camptodactyly and club foot in a Kenyan neonat…
Börjeson-Forssman-Lehmann syndrome: A case report.
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Study of Selected X-linked Disorders: Goltz Syndrome
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