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: C1275303
Disease: Erythrodermic mycosis fungoides
Erythrodermic mycosis fungoides 		1 0 1 2.8E-02 0 0
CUI: C1832162
Disease: HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY
HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY 		1 0 1 2.8E-02 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges 		1 0 1 2.8E-02 0 0
CUI: C1837008
Disease: PREMATURE OVARIAN FAILURE 3 (disorder)
PREMATURE OVARIAN FAILURE 3 (disorder) 		1 0 1 2.8E-02 0 0
CUI: C1843096
Disease: Acrocapitofemoral Dysplasia
Acrocapitofemoral Dysplasia 		1 0 1 2.8E-02 0 0
CUI: C1843105
Disease: Enlargement of the distal femoral epiphysis
Enlargement of the distal femoral epiphysis 		1 0 1 2.8E-02 0 0
CUI: C1843632
Disease: LEPROSY, SUSCEPTIBILITY TO, 2
LEPROSY, SUSCEPTIBILITY TO, 2 		1 0 1 2.8E-02 0 0
CUI: C1846157
Disease: Cone-shaped capital femoral epiphysis
Cone-shaped capital femoral epiphysis 		1 0 1 2.8E-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 2.8E-02 0 0
CUI: C1856778
Disease: Widely patent coronal suture
Widely patent coronal suture 		1 0 1 2.8E-02 0 0
CUI: C1857041
Disease: Ectodermal dysplasia, ectrodactyly, and macular dystrophy
Ectodermal dysplasia, ectrodactyly, and macular dystrophy 		1 0 1 2.8E-02 0 0
CUI: C1862261
Disease: BPES type II
BPES type II 		1 0 1 2.8E-02 0 0
CUI: C1862262
Disease: Bpes With Ovarian Failure
Bpes With Ovarian Failure 		1 0 1 2.8E-02 0 0
CUI: C1862263
Disease: Bpes Without Ovarian Failure
Bpes Without Ovarian Failure 		1 0 1 2.8E-02 0 0
CUI: C1862264
Disease: Bpes With Duane Retraction Syndrome
Bpes With Duane Retraction Syndrome 		1 0 1 2.8E-02 0 0
CUI: C1863307
Disease: Acropectorovertebral Dysplasia, F-Form
Acropectorovertebral Dysplasia, F-Form 		1 0 1 2.8E-02 0 0
CUI: C1879643
Disease: Adult Type Granulosa Cell Tumor
Adult Type Granulosa Cell Tumor 		1 0 1 2.8E-02 0 0
CUI: C1970106
Disease: Bpes, Type I, Autosomal Recessive
Bpes, Type I, Autosomal Recessive 		1 0 1 2.8E-02 0 0
CUI: C1970160
Disease: Epilepsy, Childhood Absence, Susceptibility To, 4
Epilepsy, Childhood Absence, Susceptibility To, 4 		1 0 1 2.8E-02 0 0
CUI: C2751535
Disease: Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet
Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet 		1 0 1 2.8E-02 0 0
CUI: C2931135
Disease: Blepharophimosis syndrome type 1
Blepharophimosis syndrome type 1 		1 0 1 2.8E-02 0 0
CUI: C2931136
Disease: Blepharophimosis syndrome type 2
Blepharophimosis syndrome type 2 		1 0 1 2.8E-02 0 0
CUI: C3150740
Disease: IMMUNODEFICIENCY, COMMON VARIABLE, 5
IMMUNODEFICIENCY, COMMON VARIABLE, 5 		1 0 1 2.8E-02 0 0
CUI: C3277849
Disease: 17,20-Lyase Deficiency, Isolated
17,20-Lyase Deficiency, Isolated 		1 0 1 2.8E-02 0 0
CUI: C3278138
Disease: FIBROCHONDROGENESIS 1
FIBROCHONDROGENESIS 1 		1 0 1 2.8E-02 0 0