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: C0542141
Disease: Paralysis radial
Paralysis radial
5 0 5 0.36 0 0
CUI: C1306600
Disease: Radial nerve palsy
Radial nerve palsy
5 0 5 0.36 0 0
CUI: C3854629
Disease: Tendon thickening
Tendon thickening
6 0 5 0.33 0 0
CUI: C0263374
Disease: Lichen striatus
Lichen striatus
7 0 5 0.31 0 0
CUI: C0398642
Disease: Montreal platelet syndrome
Montreal platelet syndrome
7 0 5 0.31 0 0
CUI: C0036457
Disease: Scrapie
Scrapie
8 0 5 0.29 0 0
CUI: C0340978
Disease: May-Hegglin anomaly
May-Hegglin anomaly
12 0 5 0.24 0 0
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Familial
22 0 6 0.20 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11
5 0 3 0.19 0 0
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia
25 0 6 0.18 0 0
CUI: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism
7 0 3 0.17 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy
7 0 3 0.17 0 0
CUI: C0814161
Disease: impaired motor coordination
impaired motor coordination
21 0 5 0.17 0 0
CUI: C1852467
Disease: Creutzfeldt-Jakob Disease, Sporadic
Creutzfeldt-Jakob Disease, Sporadic
57 23 10 0.16 1 4.2E-02
CUI: C0028841
Disease: Ocular Hypotension
Ocular Hypotension
22 0 5 0.16 0 0
CUI: C0263725
Disease: Hemophilic arthropathy
Hemophilic arthropathy
22 0 5 0.16 0 0
Cerebellar Ataxia and Hypogonadotropic Hypogonadism
8 0 3 0.16 0 0
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma
8 0 3 0.16 0 0
CUI: C4310512
Disease: Sporadic CJD
Sporadic CJD
30 17 6 0.16 1 5.6E-02
CUI: C0017609
Disease: Glaucoma, Neovascular
Glaucoma, Neovascular
23 0 5 0.16 0 0
New Variant Creutzfeldt-Jakob Disease
23 0 5 0.16 0 0
Iatrogenic Jakob-Creutzfeldt disease
3 0 2 0.13 0 0
CUI: C2900450
Disease: Other Creutzfeldt-Jakob disease
Other Creutzfeldt-Jakob disease
37 18 6 0.13 1 5.3E-02
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder)
13 0 3 0.12 0 0
CUI: C1801950
Disease: Opitz-G syndrome, type 2
Opitz-G syndrome, type 2
13 0 3 0.12 0 0