Source: CURATED ×
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: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID 		2 0 2 1.00 0 0
CUI: C0346303
Disease: Thyrotroph adenoma
Thyrotroph adenoma 		1 0 1 0.50 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 0.50 0 0
CUI: C1863340
Disease: PITUITARY ADENOMA PREDISPOSITION (disorder)
PITUITARY ADENOMA PREDISPOSITION (disorder) 		1 0 1 0.50 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 0.50 0 0
CUI: C2931210
Disease: Usher syndrome, type 1F
Usher syndrome, type 1F 		1 0 1 0.50 0 0
CUI: C4539685
Disease: PITUITARY ADENOMA 5, MULTIPLE TYPES
PITUITARY ADENOMA 5, MULTIPLE TYPES 		1 0 1 0.50 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		5 0 2 0.40 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 2 0.40 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 2 0.40 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		5 0 2 0.40 0 0
CUI: C0009197
Disease: Cochlear Diseases
Cochlear Diseases 		2 0 1 0.33 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		6 0 2 0.33 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		2 0 1 0.33 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		7 0 2 0.29 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		4 0 1 0.20 0 0
CUI: C0221406
Disease: Pituitary-dependent Cushing's disease
Pituitary-dependent Cushing's disease 		5 0 1 0.17 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		5 0 1 0.17 0 0
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome 		6 0 1 0.14 0 0
CUI: C0033375
Disease: Prolactinoma
Prolactinoma 		6 0 1 0.14 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		7 0 1 0.12 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		13 0 1 7.1E-02 0 0
CUI: C0004681
Disease: Bagassosis
Bagassosis 		14 0 1 6.7E-02 0 0
CUI: C0032273
Disease: Pneumoconiosis
Pneumoconiosis 		14 0 1 6.7E-02 0 0
CUI: C0011052
Disease: Prelingual Deafness
Prelingual Deafness 		20 0 1 4.8E-02 0 0