FOXN1, forkhead box N1, 8456

N. diseases: 60; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease CTD_human
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease GENOMICS_ENGLAND
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 CausalMutation disease CLINVAR
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease GENOMICS_ENGLAND
CUI: C0002170
Disease: Alopecia
Alopecia 		0.140 Biomarker disease HPO
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		0.130 Biomarker disease HPO
CUI: C0685894
Disease: Congenital absence of thymus
Congenital absence of thymus 		0.130 GeneticVariation disease CLINVAR
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation disease CLINVAR
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		0.100 Biomarker group HPO
CUI: C0150993
Disease: Pitting of nails
Pitting of nails 		0.100 Biomarker phenotype HPO
CUI: C0423820
Disease: Ridged nails
Ridged nails 		0.100 Biomarker phenotype HPO
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly 		0.100 GeneticVariation disease CLINVAR
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia 		0.100 Biomarker disease HPO
CUI: C4024723
Disease: Decreased proportion circulating T-helper cells
Decreased proportion circulating T-helper cells 		0.100 Biomarker phenotype HPO
CUI: C4025175
Disease: Congenital alopecia totalis
Congenital alopecia totalis 		0.100 Biomarker disease HPO
CUI: C4025208
Disease: Severe T-cell immunodeficiency
Severe T-cell immunodeficiency 		0.100 GeneticVariation disease CLINVAR
CUI: C4025208
Disease: Severe T-cell immunodeficiency
Severe T-cell immunodeficiency 		0.100 Biomarker disease HPO
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease MGD Thymus dysgenesis in nude (nu nu) mice. 5493276 1970
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker disease MGD Thymus dysgenesis in nude (nu nu) mice. 5493276 1970
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker disease MGD Thymus dysgenesis in nude (nu nu) mice. 5493276 1970
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease MGD Absence of thymus in a mouse mutant. 5639157 1968
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker disease MGD Absence of thymus in a mouse mutant. 5639157 1968
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		0.200 Biomarker disease MGD Absence of thymus in a mouse mutant. 5639157 1968
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		0.910 Biomarker disease MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127 1969
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.230 Biomarker disease MGD The lymphoid tissues in mice with congenital aplasia of the thymus. 5784127 1969