T-cell immunodeficiency, congenital alopecia, and nail dystrophy

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Subtype of: T-cell immunodeficiency
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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
MONDO_0011132
FOXN1 Causal
10206641 11159512 15180707 20978268 21507891 25173801 28077132 28636882 29593714 31447097 31566583 8911612
ClinGen, Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with T-cell immunodeficiency, congenital alopecia, and nail dystrophy.
5 View disease cluster →
T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. T-cell immunodeficiency 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. T-B+ severe combined immunodeficiency 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. Pharyngeal disorder 1 shared geneFOXN1 Related via 1 shared gene including FOXN1. Severe combined immunodeficiency 1 shared geneFOXN1 Related via 1 shared gene including FOXN1.