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: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 5 8.9E-02 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 4 8.5E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 2 8.3E-02 0 0
CUI: C3887558
Disease: Hemophagocytic Syndrome
Hemophagocytic Syndrome 		25 0 3 8.3E-02 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis 		13 0 2 8.0E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 2 8.0E-02 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		13 0 2 8.0E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 6 7.9E-02 0 0
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome 		41 0 4 7.8E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 7.1E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 7.1E-02 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1304147
Disease: Retention hyperkeratosis
Retention hyperkeratosis 		1 0 1 7.1E-02 0 0
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 16 1 7.1E-02 1 3.8E-02
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 7.1E-02 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 7.1E-02 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
Deafness, Autosomal Recessive 18 		1 0 1 7.1E-02 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 7.1E-02 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 7.1E-02 0 0
CUI: C1969516
Disease: Aberrant melanosome maturation
Aberrant melanosome maturation 		1 0 1 7.1E-02 0 0
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 7.1E-02 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 7.1E-02 0 0