Dyskeratosis congenita, autosomal recessive 8

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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 recessive 8
MONDO_0859319
DCLRE1B Causal
20479256 35007328
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Dyskeratosis congenita, autosomal recessive 8.
5 View disease cluster →
Hoyeraal hreidarsson syndrome 1 shared geneDCLRE1B Related via 1 shared gene including DCLRE1B. Dyskeratosis congenita 1 shared geneDCLRE1B Related via 1 shared gene including DCLRE1B. Fanconi anemia 1 shared geneDCLRE1B Related via 1 shared gene including DCLRE1B. Hereditary spastic paraplegia 1 shared geneDCLRE1B Related via 1 shared gene including DCLRE1B. Spastic paraplegia 1 shared geneDCLRE1B Related via 1 shared gene including DCLRE1B.