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: 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
CUI: C1862264
Disease: Bpes With Duane Retraction Syndrome
Bpes With Duane Retraction Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1879643
Disease: Adult Type Granulosa Cell Tumor
Adult Type Granulosa Cell Tumor 		1 0 1 7.1E-02 0 0
CUI: C1970106
Disease: Bpes, Type I, Autosomal Recessive
Bpes, Type I, Autosomal Recessive 		1 0 1 7.1E-02 0 0
CUI: C2829265
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 86
DEAFNESS, AUTOSOMAL RECESSIVE 86 		1 0 1 7.1E-02 0 0
CUI: C2931135
Disease: Blepharophimosis syndrome type 1
Blepharophimosis syndrome type 1 		1 0 1 7.1E-02 0 0
CUI: C2931136
Disease: Blepharophimosis syndrome type 2
Blepharophimosis syndrome type 2 		1 0 1 7.1E-02 0 0
CUI: C3279660
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 29
DEAFNESS, AUTOSOMAL RECESSIVE 29 		1 0 1 7.1E-02 0 0
CUI: C3280471
Disease: OVARIAN DYSGENESIS 3
OVARIAN DYSGENESIS 3 		1 0 1 7.1E-02 0 0
CUI: C3714208
Disease: Blepharophimosis, Ptosis, and Epicanthus Inversus Type II
Blepharophimosis, Ptosis, and Epicanthus Inversus Type II 		1 0 1 7.1E-02 0 0
CUI: C3808414
Disease: PERRAULT SYNDROME 3
PERRAULT SYNDROME 3 		1 0 1 7.1E-02 0 0
CUI: C3809173
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16 		1 0 1 7.1E-02 0 0
CUI: C3809181
Disease: Caused by mutation in the TBC1 domain family, member 24 gene (TBC1D24, 613577.0004)
Caused by mutation in the TBC1 domain family, member 24 gene (TBC1D24, 613577.0004) 		1 0 1 7.1E-02 0 0
CUI: C3892048
Disease: DEAFNESS, AUTOSOMAL DOMINANT 65
DEAFNESS, AUTOSOMAL DOMINANT 65 		1 0 1 7.1E-02 0 0