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: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I 		80 0 14 7.9E-02 0 0
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis 		176 0 21 7.9E-02 0 0
CUI: C1266050
Disease: Poorly Differentiated Thyroid Carcinoma
Poorly Differentiated Thyroid Carcinoma 		54 0 12 7.8E-02 0 0
CUI: C0022548
Disease: Keloid
Keloid 		165 0 20 7.8E-02 0 0
CUI: C0041974
Disease: Urethral Stenosis
Urethral Stenosis 		41 0 11 7.8E-02 0 0
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		85 0 14 7.7E-02 0 0
CUI: C1867441
Disease: Pterygium Of Conjunctiva And Cornea
Pterygium Of Conjunctiva And Cornea 		169 0 20 7.7E-02 0 0
CUI: C4520843
Disease: Pterygium of eye
Pterygium of eye 		169 0 20 7.7E-02 0 0
CUI: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic 		185 0 21 7.6E-02 0 0
CUI: C0796070
Disease: MICROPHTHALMIA, SYNDROMIC 7
MICROPHTHALMIA, SYNDROMIC 7 		46 0 11 7.5E-02 0 0
CUI: C3279947
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 		77 0 13 7.4E-02 0 0
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia 		78 0 13 7.4E-02 0 0
CUI: C0042025
Disease: Urinary Stress Incontinence
Urinary Stress Incontinence 		79 0 13 7.3E-02 0 0
CUI: C0423820
Disease: Ridged nails
Ridged nails 		22 0 9 7.3E-02 0 0
CUI: C0040021
Disease: Thromboangiitis Obliterans
Thromboangiitis Obliterans 		127 0 16 7.2E-02 0 0
CUI: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy 		142 0 17 7.2E-02 0 0
CUI: C0333983
Disease: Hyperplastic Polyp
Hyperplastic Polyp 		204 0 21 7.1E-02 0 0
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology 		39 0 10 7.1E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 40 7.1E-02 0 0
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		85 0 13 7.1E-02 0 0
CUI: C1857656
Disease: Prematurely aged appearance
Prematurely aged appearance 		40 0 10 7.1E-02 0 0
CUI: C0399440
Disease: Hereditary gingival fibromatosis
Hereditary gingival fibromatosis 		86 0 13 7.1E-02 0 0
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation 		73 0 12 7.0E-02 0 0
CUI: C2931367
Disease: Thyroid cancer, follicular
Thyroid cancer, follicular 		58 0 11 7.0E-02 0 0
CUI: C2717836
Disease: Steroid Sulfatase Deficiency Disease
Steroid Sulfatase Deficiency Disease 		181 0 19 7.0E-02 0 0