t-cell immunodeficiency, congenital alopecia, and nail dystrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
FOXN1 Causal
21507891 25173801 28636882 10206641 31566583 20978268
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with t-cell immunodeficiency, congenital alopecia, and nail dystrophy.
4 View disease cluster →
Pharyngeal disorder 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. Combined immunodeficiency disease 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. Severe combined immunodeficiency 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. Autism 1 shared geneFOXN1 Related via 1 shared gene including FOXN1.