immunodeficiency-centromeric instability-facial anomalies syndrome 1

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Immunodeficiency-centromeric instability-facial anomalies syndrome 1
DNMT3B Causal
27734333 10555141 15580563 11102980 10588719 10647011 21120685
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with immunodeficiency-centromeric instability-facial anomalies syndrome 1.
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Facioscapulohumeral muscular dystrophy 1 shared geneDNMT3B Related via 1 shared gene including DNMT3B. Immunodeficiency-centromeric instability-facial anomalies syndrome 1 shared geneDNMT3B Related via 1 shared gene including DNMT3B. Kabuki syndrome 1 shared geneDNMT3B Related via 1 shared gene including DNMT3B. Myelodysplastic syndrome 1 shared geneDNMT3B Related via 1 shared gene including DNMT3B. Female infertility 1 shared geneDNMT3B Related via 1 shared gene including DNMT3B.