Congenital leukocyte adherence deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL LEUKOCYTE ADHERENCE DEFICIENCY
C0272187
FERMT3 Unknown — Disgenet
ITGB2 Unknown — Disgenet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital leukocyte adherence deficiency.
5 View disease cluster →
Leukocyte adhesion deficiency 2 shared genesFERMT3, ITGB2 Related via 2 shared genes including FERMT3, ITGB2. Leukocyte disorders 1 shared geneITGB2 Related via 1 shared gene including ITGB2. Skin ulcer 1 shared geneITGB2 Related via 1 shared gene including ITGB2. Platelet disorder 1 shared geneFERMT3 Related via 1 shared gene including FERMT3. Coronary restenosis 1 shared geneITGB2 Related via 1 shared gene including ITGB2.