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: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		68 8 44 0.52 3 0.33
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		69 0 28 0.28 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		57 0 20 0.21 0 0
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		85 0 24 0.20 0 0
CUI: C1832446
Disease: Sparse eyebrow
Sparse eyebrow 		31 6 14 0.18 1 0.11
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		35 0 14 0.17 0 0
CUI: C0423867
Disease: Fine hair
Fine hair 		69 0 19 0.17 0 0
CUI: C1873509
Disease: Hypotrichosis of the scalp
Hypotrichosis of the scalp 		12 0 10 0.16 0 0
CUI: C0263490
Disease: Brittle hair
Brittle hair 		45 1 14 0.15 1 0.25
CUI: C4721530
Disease: Congenital hypotrichia
Congenital hypotrichia 		19 4 9 0.13 1 0.14
CUI: C1843005
Disease: Absent eyelashes
Absent eyelashes 		21 0 9 0.12 0 0
CUI: C3279947
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 		77 0 15 0.12 0 0
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia 		78 0 15 0.12 0 0
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 14 0.12 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 9 0.12 0 0
CUI: C0431448
Disease: Absent eyebrow
Absent eyebrow 		19 0 8 0.11 0 0
CUI: C4021956
Disease: Aplasia/Hypoplasia of the eyebrow
Aplasia/Hypoplasia of the eyebrow 		52 0 11 0.11 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		69 0 12 0.10 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair 		112 9 16 0.10 1 8.3E-02
CUI: C1857206
Disease: Sparse lateral eyebrow
Sparse lateral eyebrow 		20 0 7 9.6E-02 0 0
CUI: C3551431
Disease: Sparse or absent eyelashes
Sparse or absent eyelashes 		13 0 6 9.0E-02 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 11 8.5E-02 0 0
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		57 0 9 8.3E-02 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 6 8.3E-02 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 6 8.3E-02 0 0