Dyskeratosis congenita, autosomal dominant 4

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Subtype of: Dyskeratosis congenita
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Dyskeratosis congenita, autosomal dominant 4
MONDO_0014076
RTEL1 Causal
23453664 23959892 23329068 24582487 23591994 29146883 30466750
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Dyskeratosis congenita, autosomal dominant 4.
5 View disease cluster →
Dyskeratosiscongenita, autosomal dominant 4 1 shared geneRTEL1 Related via 1 shared gene including RTEL1. Dc type 4 and 5 1 shared geneRTEL1 Related via 1 shared gene including RTEL1. Dyskeratosis congenita, autosomal recessive 5 1 shared geneRTEL1 Related via 1 shared gene including RTEL1. X-linked dyskeratosis congenita 1 shared geneRTEL1 Related via 1 shared gene including RTEL1. Telomere syndrome 1 shared geneRTEL1 Related via 1 shared gene including RTEL1.