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: C3554449
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 		1 0 1 9.1E-02 0 0
CUI: C3887926
Disease: CATARACT 32, MULTIPLE TYPES
CATARACT 32, MULTIPLE TYPES 		1 0 1 9.1E-02 0 0
CUI: C4013950
Disease: IMMUNODEFICIENCY 31A
IMMUNODEFICIENCY 31A 		1 0 1 9.1E-02 0 0
CUI: C4015848
Disease: APOLIPOPROTEIN C-III, NONGLYCOSYLATED PHENOTYPE
APOLIPOPROTEIN C-III, NONGLYCOSYLATED PHENOTYPE 		1 0 1 9.1E-02 0 0
CUI: C4020971
Disease: Abnormality of lower limb joint
Abnormality of lower limb joint 		1 0 1 9.1E-02 0 0
CUI: C4021625
Disease: Spinal stenosis with reduced interpedicular distance
Spinal stenosis with reduced interpedicular distance 		1 0 1 9.1E-02 0 0
CUI: C4023443
Disease: Absent antitragus
Absent antitragus 		1 0 1 9.1E-02 0 0
CUI: C4025083
Disease: Thimble-shaped middle phalanges of hand
Thimble-shaped middle phalanges of hand 		1 0 1 9.1E-02 0 0
CUI: C4025834
Disease: Abnormal amplitude of pattern reversal visual evoked potentials
Abnormal amplitude of pattern reversal visual evoked potentials 		1 0 1 9.1E-02 0 0
CUI: C4054251
Disease: Pancreaticobiliary Malunion
Pancreaticobiliary Malunion 		1 0 1 9.1E-02 0 0
CUI: C4087190
Disease: Sulcus vocalis
Sulcus vocalis 		1 0 1 9.1E-02 0 0
CUI: C4225163
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE) 		1 0 1 9.1E-02 0 0
CUI: C4225629
Disease: SEVERE ACHONDRODYSPLASIA WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS
SEVERE ACHONDRODYSPLASIA WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS 		1 1 1 9.1E-02 1 5.9E-02
CUI: C4275164
Disease: Autosomal dominant optic atrophy plus syndrome
Autosomal dominant optic atrophy plus syndrome 		1 0 1 9.1E-02 0 0
CUI: C4527240
Disease: Pleomorphic lobular carcinoma in situ of breast
Pleomorphic lobular carcinoma in situ of breast 		1 0 1 9.1E-02 0 0
CUI: C4539767
Disease: EXUDATIVE VITREORETINOPATHY 7
EXUDATIVE VITREORETINOPATHY 7 		1 0 1 9.1E-02 0 0
CUI: C4684845
Disease: Pulmonary Artery Intimal Sarcoma
Pulmonary Artery Intimal Sarcoma 		1 0 1 9.1E-02 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		14 29 2 8.7E-02 1 2.2E-02
CUI: C0034535
Disease: Radiation Syndrome
Radiation Syndrome 		14 0 2 8.7E-02 0 0
CUI: C0011645
Disease: Dermatosis Papulosa Nigra
Dermatosis Papulosa Nigra 		2 0 1 8.3E-02 0 0
CUI: C0025490
Disease: Mesonephroma
Mesonephroma 		2 0 1 8.3E-02 0 0
CUI: C0040262
Disease: Tinea Versicolor
Tinea Versicolor 		2 0 1 8.3E-02 0 0
CUI: C0206646
Disease: Fibromatosis, Abdominal
Fibromatosis, Abdominal 		2 0 1 8.3E-02 0 0
CUI: C0221061
Disease: Behr syndrome
Behr syndrome 		2 0 1 8.3E-02 0 0
CUI: C0263419
Disease: Reactive perforating collagenosis
Reactive perforating collagenosis 		2 0 1 8.3E-02 0 0