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: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC 		3 0 2 0.14 0 0
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D 		4 0 2 0.13 0 0
CUI: C3806221
Disease: Giant melanosomes in melanocytes
Giant melanosomes in melanocytes 		4 0 2 0.13 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 6 0.12 0 0
CUI: C4022758
Disease: Mild hearing impairment
Mild hearing impairment 		6 0 2 0.12 0 0
CUI: C2676026
Disease: Optic nerve dysplasia
Optic nerve dysplasia 		7 0 2 0.11 0 0
CUI: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID 		8 0 2 0.11 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 11 9.4E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 2 8.7E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 2 8.3E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 2 8.3E-02 0 0
CUI: C3668948
Disease: Circling behavior
Circling behavior 		14 0 2 8.0E-02 0 0
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 7.7E-02 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation 		1 0 1 7.7E-02 0 0
CUI: C0346977
Disease: Secondary malignant neoplasm of spleen
Secondary malignant neoplasm of spleen 		1 0 1 7.7E-02 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome 		1 0 1 7.7E-02 0 0
CUI: C1313983
Disease: Acute contagious conjunctivitis
Acute contagious conjunctivitis 		1 0 1 7.7E-02 0 0
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 0 1 7.7E-02 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 7.7E-02 0 0
CUI: C1847024
Disease: ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1847132
Disease: ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE 		1 0 1 7.7E-02 0 0
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
Deafness, Autosomal Recessive 18 		1 0 1 7.7E-02 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 7.7E-02 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 7.7E-02 0 0
CUI: C2673954
Disease: Absent skin pigmentation
Absent skin pigmentation 		1 0 1 7.7E-02 0 0