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: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 11 0.61 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 11 0.48 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 5 0.38 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 5 0.38 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		13 0 7 0.37 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 7 0.35 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 12 0.32 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 11 0.26 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 0 7 0.24 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 5 0.23 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 11 0.22 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 5 0.21 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 6 0.21 0 0
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 3 0.17 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 11 0.16 0 0
CUI: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 2 0.15 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 2 0.15 0 0
CUI: C0078923
Disease: Albinism, Yellow-Mutant
Albinism, Yellow-Mutant 		2 0 2 0.15 0 0
CUI: C1863198
Disease: ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder) 		2 0 2 0.15 0 0
CUI: C3152204
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 		2 0 2 0.15 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 2 0.15 0 0
CUI: C4525234
Disease: Xiphophorus Melanoma
Xiphophorus Melanoma 		2 0 2 0.15 0 0
CUI: C1845069
Disease: ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder) 		3 0 2 0.14 0 0
CUI: C1848604
Disease: USHER SYNDROME, TYPE IC
USHER SYNDROME, TYPE IC 		3 0 2 0.14 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 3 0.14 0 0