Chromosome 16p11.2 deletion syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CHROMOSOME 16P11.2 DELETION SYNDROME, 220-KB
C3150701
SH2B1 Unknown — Disgenet
CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB
C3150154
SFTPA1 Unknown — Disgenet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Chromosome 16p11.2 deletion syndrome.
5 View disease cluster →
interstitial lung disease 1 1 shared geneSFTPA1 Related via 1 shared gene including SFTPA1. Chromosome 16p11.2 microdeletion syndrome 1 shared geneSH2B1 Related via 1 shared gene including SH2B1. Bronchopulmonary dysplasia 1 shared geneSFTPA1 Related via 1 shared gene including SFTPA1. Interstitial lung disease 1 shared geneSFTPA1 Related via 1 shared gene including SFTPA1. Idiopathic pulmonary fibrosis 1 shared geneSFTPA1 Related via 1 shared gene including SFTPA1.