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: C0232769
Disease: Abnormal gallbladder function
Abnormal gallbladder function 		3 0 2 0.67 0 0
CUI: C1853249
Disease: SPINOCEREBELLAR ATAXIA 28
SPINOCEREBELLAR ATAXIA 28 		4 0 2 0.50 0 0
CUI: C4540277
Disease: FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION
FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION 		1 0 1 0.50 0 0
CUI: C0428465
Disease: Serum lipids high (finding)
Serum lipids high (finding) 		7 0 2 0.29 0 0
CUI: C0030583
Disease: Parotitis
Parotitis 		8 0 2 0.25 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 0 1 0.17 0 0
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 0 1 0.14 0 0
CUI: C1855650
Disease: Birth length less than 3rd percentile
Birth length less than 3rd percentile 		21 0 2 9.5E-02 0 0
CUI: C4551521
Disease: Kinetic tremor
Kinetic tremor 		13 0 1 7.1E-02 0 0
CUI: C0232608
Disease: Nasal regurgitation
Nasal regurgitation 		14 0 1 6.7E-02 0 0
CUI: C0376175
Disease: Bell Palsy
Bell Palsy 		15 0 1 6.2E-02 0 0
CUI: C4023180
Disease: Type 1 muscle fiber atrophy
Type 1 muscle fiber atrophy 		16 0 1 5.9E-02 0 0
CUI: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 1 5.6E-02 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 1 5.6E-02 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy 		17 0 1 5.6E-02 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome 		17 0 1 5.6E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 1 5.3E-02 0 0
CUI: C0234518
Disease: Slurred speech
Slurred speech 		39 0 2 5.1E-02 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 2 5.1E-02 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 1 4.8E-02 0 0
CUI: C0751779
Disease: Action Myoclonus-Renal Failure Syndrome
Action Myoclonus-Renal Failure Syndrome 		20 0 1 4.8E-02 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 0 1 4.8E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 0 2 4.5E-02 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 1 4.5E-02 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 2 4.4E-02 0 0