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: C0373745
Disease: Vitamin A measurement
Vitamin A measurement 		1 0 1 0.25 0 0
CUI: C2675659
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 		1 0 1 0.25 0 0
CUI: C4225667
Disease: CHROMOSOME 16p13.2 DELETION SYNDROME
CHROMOSOME 16p13.2 DELETION SYNDROME 		1 0 1 0.25 0 0
CUI: C3554593
Disease: RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME
RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME 		2 0 1 0.20 0 0
CUI: C4225330
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10 		2 0 1 0.20 0 0
CUI: C4021650
Disease: Short third metatarsal
Short third metatarsal 		3 0 1 0.17 0 0
CUI: C4024881
Disease: Few cafe-au-lait spots
Few cafe-au-lait spots 		3 0 1 0.17 0 0
CUI: C4021649
Disease: Short fifth metatarsal
Short fifth metatarsal 		4 0 1 0.14 0 0
CUI: C4023802
Disease: Hyperextensibility of the knee
Hyperextensibility of the knee 		4 0 1 0.14 0 0
CUI: C4025212
Disease: Autonomic bladder dysfunction
Autonomic bladder dysfunction 		5 0 1 0.12 0 0
CUI: C1848514
Disease: Short fourth metatarsal
Short fourth metatarsal 		8 0 1 9.1E-02 0 0
CUI: C4021217
Disease: EEG with generalized slow activity
EEG with generalized slow activity 		8 0 1 9.1E-02 0 0
CUI: C0233407
Disease: Disorientation
Disorientation 		12 0 1 6.7E-02 0 0
CUI: C0266036
Disease: Macrodontia
Macrodontia 		12 0 1 6.7E-02 0 0
CUI: C4072904
Disease: Secondary Caesarian section
Secondary Caesarian section 		13 0 1 6.2E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 0 1 5.9E-02 0 0
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		15 0 1 5.6E-02 0 0
CUI: C0002994
Disease: Angioedema
Angioedema 		18 0 1 4.8E-02 0 0
CUI: C0024449
Disease: Mycetoma
Mycetoma 		19 0 1 4.5E-02 0 0
CUI: C0040247
Disease: Tinea
Tinea 		21 0 1 4.2E-02 0 0
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
CRANIOSYNOSTOSIS, TYPE 2 		23 0 1 3.8E-02 0 0
CUI: C1334815
Disease: Multi-centric Castleman's Disease
Multi-centric Castleman's Disease 		29 0 1 3.1E-02 0 0
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		30 0 1 3.0E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 0 1 2.9E-02 0 0
CUI: C0020580
Disease: Hypesthesia
Hypesthesia 		33 0 1 2.8E-02 0 0