Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0858699
Disease: Skin keratosis
Skin keratosis 		1 0 1 1.00 0 0
CUI: C1866426
Disease: T-cell immunodeficiency, congenital alopecia and nail dystrophy
T-cell immunodeficiency, congenital alopecia and nail dystrophy 		1 0 1 1.00 0 0
CUI: C4024723
Disease: Decreased proportion circulating T-helper cells
Decreased proportion circulating T-helper cells 		1 0 1 1.00 0 0
CUI: C4025175
Disease: Congenital alopecia totalis
Congenital alopecia totalis 		2 0 1 0.50 0 0
CUI: C0265992
Disease: alopecia congenita
alopecia congenita 		3 0 1 0.33 0 0
CUI: C3495530
Disease: Congenital alopecia X-linked
Congenital alopecia X-linked 		3 0 1 0.33 0 0
CUI: C4025208
Disease: Severe T-cell immunodeficiency
Severe T-cell immunodeficiency 		5 0 1 0.20 0 0
CUI: C0235864
Disease: Congenital hypertrichosis lanuginosa
Congenital hypertrichosis lanuginosa 		6 0 1 0.17 0 0
CUI: C0685894
Disease: Congenital absence of thymus
Congenital absence of thymus 		6 0 1 0.17 0 0
CUI: C2936812
Disease: Congenital hypertrichosis
Congenital hypertrichosis 		6 0 1 0.17 0 0
CUI: C0150993
Disease: Pitting of nails
Pitting of nails 		8 0 1 0.12 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 1.0E-01 0 0
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia 		17 0 1 5.9E-02 0 0
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis 		19 0 1 5.3E-02 0 0
CUI: C0423820
Disease: Ridged nails
Ridged nails 		22 0 1 4.5E-02 0 0
CUI: C0014458
Disease: Eosinophilia, Tropical
Eosinophilia, Tropical 		24 0 1 4.2E-02 0 0
CUI: C0040115
Disease: Thymus Hyperplasia
Thymus Hyperplasia 		30 0 1 3.3E-02 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 1 2.9E-02 0 0
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		44 0 1 2.3E-02 0 0
CUI: C0265354
Disease: CHARGE Syndrome
CHARGE Syndrome 		49 0 1 2.0E-02 0 0
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly 		49 0 1 2.0E-02 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly 		59 0 1 1.7E-02 0 0
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		61 0 1 1.6E-02 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 1 1.2E-02 0 0
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		111 0 1 9.0E-03 0 0