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: C2315430
Disease: Orthostatic tremor
Orthostatic tremor 		2 0 2 0.14 0 0
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		2 0 2 0.14 0 0
CUI: C3554105
Disease: PERRAULT SYNDROME 2
PERRAULT SYNDROME 2 		2 7 2 0.14 2 0.12
CUI: C3809105
Disease: PERRAULT SYNDROME 4
PERRAULT SYNDROME 4 		2 8 2 0.14 1 5.6E-02
CUI: C4551721
Disease: PERRAULT SYNDROME 1
PERRAULT SYNDROME 1 		2 0 2 0.14 0 0
CUI: C0342510
Disease: Ovarian dysgenesis
Ovarian dysgenesis 		6 0 2 0.11 0 0
CUI: C1849096
Disease: Infantile onset spinocerebellar ataxia
Infantile onset spinocerebellar ataxia 		6 10 2 0.11 1 5.0E-02
CUI: C1401084
Disease: Ovarian Insufficiency
Ovarian Insufficiency 		9 0 2 9.5E-02 0 0
CUI: C2609059
Disease: Antisynthetase syndrome
Antisynthetase syndrome 		9 0 2 9.5E-02 0 0
CUI: C1842138
Disease: Progressive hearing impairment
Progressive hearing impairment 		14 0 2 7.7E-02 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 4 7.5E-02 0 0
CUI: C0085543
Disease: Epilepsia Partialis Continua
Epilepsia Partialis Continua 		15 0 2 7.4E-02 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 2 7.4E-02 0 0
CUI: C0266572
Disease: Congenital anomaly of eyelid
Congenital anomaly of eyelid 		1 0 1 7.1E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 7.1E-02 0 0
CUI: C0585006
Disease: Deficiency of enoyl-CoA hydratase
Deficiency of enoyl-CoA hydratase 		1 0 1 7.1E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 7.1E-02 0 0
CUI: C1533628
Disease: Pseudo-Zellweger syndrome
Pseudo-Zellweger syndrome 		1 0 1 7.1E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 7.1E-02 0 0
CUI: C1837008
Disease: PREMATURE OVARIAN FAILURE 3 (disorder)
PREMATURE OVARIAN FAILURE 3 (disorder) 		1 0 1 7.1E-02 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 7.1E-02 0 0
CUI: C1854128
Disease: BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE II WITH DUANE RETRACTION SYNDROME
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE II WITH DUANE RETRACTION SYNDROME 		1 0 1 7.1E-02 0 0
CUI: C1862261
Disease: BPES type II
BPES type II 		1 0 1 7.1E-02 0 0
CUI: C1862262
Disease: Bpes With Ovarian Failure
Bpes With Ovarian Failure 		1 0 1 7.1E-02 0 0
CUI: C1862263
Disease: Bpes Without Ovarian Failure
Bpes Without Ovarian Failure 		1 0 1 7.1E-02 0 0