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: C0520680
Disease: Sleep Apnea, Central
Sleep Apnea, Central 		122 17 73 0.57 10 0.20
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		85 11 21 0.15 1 1.9E-02
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 11 0.12 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 14 0.12 0 0
CUI: C0002963
Disease: Angina Pectoris, Variant
Angina Pectoris, Variant 		26 0 11 0.12 0 0
CUI: C1955934
Disease: Trichothiodystrophy Syndromes
Trichothiodystrophy Syndromes 		33 0 11 0.11 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 21 0.11 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 9 0.11 0 0
CUI: C4304411
Disease: Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum and Cockayne syndrome complex 		10 0 8 9.8E-02 0 0
CUI: C0271160
Disease: Cortical cataract
Cortical cataract 		69 0 13 9.6E-02 0 0
CUI: C1968564
Disease: Defective DNA repair after ultraviolet radiation damage
Defective DNA repair after ultraviolet radiation damage 		12 0 8 9.5E-02 0 0
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		15 0 8 9.2E-02 0 0
CUI: C0014390
Disease: Entropion
Entropion 		18 0 8 8.9E-02 0 0
CUI: C0022568
Disease: Keratitis
Keratitis 		156 0 19 8.8E-02 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		20 0 8 8.7E-02 0 0
CUI: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		34 0 9 8.6E-02 0 0
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 10 8.3E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 11 7.9E-02 0 0
CUI: C1883018
Disease: Severe Aplastic Anemia
Severe Aplastic Anemia 		70 0 11 7.9E-02 0 0
CUI: C3887551
Disease: Memory dysfunction
Memory dysfunction 		70 0 11 7.9E-02 0 0
CUI: C0151514
Disease: Atrophic condition of skin
Atrophic condition of skin 		111 0 14 7.9E-02 0 0
CUI: C0016689
Disease: Freckles
Freckles 		45 0 9 7.8E-02 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		91 3 12 7.5E-02 1 2.3E-02
CUI: C0751038
Disease: Cockayne Syndrome, Type II
Cockayne Syndrome, Type II 		34 0 8 7.5E-02 0 0
CUI: C0917804
Disease: Arteriovenous Malformations, Cerebral
Arteriovenous Malformations, Cerebral 		35 0 8 7.5E-02 0 0