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: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 20 0.18 0 0
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		15 0 15 0.18 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 35 32 0.17 1 2.2E-02
CUI: C0751038
Disease: Cockayne Syndrome, Type II
Cockayne Syndrome, Type II 		34 0 17 0.17 0 0
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I 		80 42 21 0.15 1 1.9E-02
CUI: C1955934
Disease: Trichothiodystrophy Syndromes
Trichothiodystrophy Syndromes 		33 0 15 0.15 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 31 13 0.14 1 2.4E-02
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 18 0.13 0 0
CUI: C0033300
Disease: Progeria
Progeria 		118 41 22 0.12 2 4.0E-02
CUI: C0271160
Disease: Cortical cataract
Cortical cataract 		69 0 16 0.12 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 10 0.11 0 0
CUI: C0231341
Disease: Premature aging syndrome
Premature aging syndrome 		136 0 22 0.11 0 0
CUI: C0014390
Disease: Entropion
Entropion 		18 0 10 0.11 0 0
CUI: C0347915
Disease: Congenital malformation syndromes associated with short stature
Congenital malformation syndromes associated with short stature 		9 0 9 0.11 0 0
CUI: C4304411
Disease: Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum and Cockayne syndrome complex 		10 0 9 0.10 0 0
CUI: C0175691
Disease: Dubowitz syndrome
Dubowitz syndrome 		12 0 9 0.10 0 0
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
CRANIOSYNOSTOSIS, TYPE 2 		23 0 10 0.10 0 0
CUI: C0520680
Disease: Sleep Apnea, Central
Sleep Apnea, Central 		122 0 18 9.5E-02 0 0
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		20 0 9 9.4E-02 0 0
CUI: C0016689
Disease: Freckles
Freckles 		45 0 11 9.2E-02 0 0
CUI: C1968564
Disease: Defective DNA repair after ultraviolet radiation damage
Defective DNA repair after ultraviolet radiation damage 		12 0 8 9.0E-02 0 0
CUI: C1857710
Disease: Progeroid facial appearance
Progeroid facial appearance 		14 0 8 8.8E-02 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		130 0 17 8.6E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 12 8.5E-02 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		20 0 8 8.2E-02 0 0