Congenital camptodactyly

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL CAMPTODACTYLY
C0685409
MED13L Unknown — Disgenet
PLOD2 Unknown — Disgenet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital camptodactyly.
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Cardiac anomalies - developmental delay - facial dysmorphism syndrome 1 shared geneMED13L Related via 1 shared gene including MED13L. Developmental delay with facial dysmorphism syndrome 1 shared geneMED13L Related via 1 shared gene including MED13L. Bowed long bones 1 shared genePLOD2 Related via 1 shared gene including PLOD2. Buruli ulcer 1 shared genePLOD2 Related via 1 shared gene including PLOD2. Congenital hypoplasia of femur 1 shared genePLOD2 Related via 1 shared gene including PLOD2.