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: C4025836
Disease: Abnormal choroid morphology
Abnormal choroid morphology 		12 0 2 7.4E-02 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 3 7.1E-02 0 0
CUI: C0152438
Disease: Sprengel deformity
Sprengel deformity 		29 0 3 7.0E-02 0 0
CUI: C1698196
Disease: Muscle Weakness Upper Limb
Muscle Weakness Upper Limb 		29 0 3 7.0E-02 0 0
CUI: C0685776
Disease: Congenital absence of mandible
Congenital absence of mandible 		14 0 2 6.9E-02 0 0
CUI: C4023383
Disease: Narrow internal auditory canal
Narrow internal auditory canal 		14 0 2 6.9E-02 0 0
CUI: C0043407
Disease: Yersinia infections
Yersinia infections 		17 0 2 6.2E-02 0 0
CUI: C1843496
Disease: Bilateral microphthalmos
Bilateral microphthalmos 		35 0 3 6.1E-02 0 0
CUI: C0025988
Disease: Microglossia
Microglossia 		19 0 2 5.9E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 5.9E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 5.9E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 5.9E-02 0 0
CUI: C0276161
Disease: Subacute adenoviral encephalitis
Subacute adenoviral encephalitis 		1 0 1 5.9E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 5.9E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 5.9E-02 0 0
CUI: C0400847
Disease: Ileal Stenosis
Ileal Stenosis 		1 0 1 5.9E-02 0 0
CUI: C0400978
Disease: Secondary sclerosing cholangitis
Secondary sclerosing cholangitis 		1 0 1 5.9E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 0 1 5.9E-02 0 0
CUI: C0544839
Disease: Macular amyloidosis
Macular amyloidosis 		1 0 1 5.9E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 5.9E-02 0 0
CUI: C1275718
Disease: Granulomatous rosacea
Granulomatous rosacea 		1 0 1 5.9E-02 0 0
CUI: C1301260
Disease: Gastrointestinal Crohn's disease
Gastrointestinal Crohn's disease 		1 0 1 5.9E-02 0 0
CUI: C1832823
Disease: Klippel-Feil anomaly
Klippel-Feil anomaly 		1 0 1 5.9E-02 0 0
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia 		1 0 1 5.9E-02 0 0
CUI: C1834013
Disease: Odontoma dysphagia syndrome
Odontoma dysphagia syndrome 		1 0 1 5.9E-02 0 0