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: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
39 104 39 1.00 104 1.00
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
39 104 39 1.00 104 1.00
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
39 104 39 1.00 104 1.00
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
91 743 39 0.43 104 0.14
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia
112 107 39 0.35 104 0.97
CUI: C0002170
Disease: Alopecia
Alopecia
491 375 34 6.9E-02 67 0.16
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
4 0 2 4.9E-02 0 0
CUI: C0432255
Disease: Geroderma osteodysplastica
Geroderma osteodysplastica
5 0 2 4.8E-02 0 0
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration
35 0 3 4.2E-02 0 0
CUI: C4021823
Disease: Ambiguous genitalia, male
Ambiguous genitalia, male
13 0 2 4.0E-02 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth
14 0 2 3.9E-02 0 0
Colorectal Traditional Serrated Adenoma
14 0 2 3.9E-02 0 0
CUI: C1840319
Disease: Redundant neck skin
Redundant neck skin
16 0 2 3.8E-02 0 0
CUI: C2697766
Disease: Interleukin 18 Measurement
Interleukin 18 Measurement
16 0 2 3.8E-02 0 0
CUI: C1846434
Disease: Hypoplastic scapulae
Hypoplastic scapulae
18 0 2 3.6E-02 0 0
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
18 10 2 3.6E-02 1 8.8E-03
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
18 11 2 3.6E-02 1 8.8E-03
Precocious exfoliation of primary tooth
20 0 2 3.5E-02 0 0
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
25 7 2 3.2E-02 1 9.1E-03
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
25 35 2 3.2E-02 1 7.2E-03
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe
26 0 2 3.2E-02 0 0
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias
29 0 2 3.0E-02 0 0
Rheumatoid Arthritis, Systemic Juvenile
30 0 2 3.0E-02 0 0
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
74 0 3 2.7E-02 0 0
CUI: C2718001
Disease: Protein Misfolding Disorders
Protein Misfolding Disorders
38 0 2 2.7E-02 0 0