Autosomal dominant combined immunodeficiency

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Combined immunodeficiency
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal dominant combined immunodeficiency due to ERBIN deficiency
656912C5925110MONDO:0958120
ERBIN Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Autosomal dominant combined immunodeficiency.
5 View disease cluster →
Combined immunodeficiency 1 shared geneERBIN Related via 1 shared gene including ERBIN. Uterine fibroid 1 shared geneERBIN Related via 1 shared gene including ERBIN. Adenoid cystic carcinoma 1 shared geneERBIN Related via 1 shared gene including ERBIN. Non-small cell lung carcinoma 1 shared geneERBIN Related via 1 shared gene including ERBIN. Scoliosis 1 shared geneERBIN Related via 1 shared gene including ERBIN.