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 2 3 0.38 1 2.4E-02
CUI: C4539685
Disease: PITUITARY ADENOMA 5, MULTIPLE TYPES
PITUITARY ADENOMA 5, MULTIPLE TYPES 		2 8 2 0.25 4 9.1E-02
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 57 2 0.20 4 4.3E-02
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D 		4 0 2 0.20 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 2 0.18 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 2 0.18 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 12 1 0.12 2 4.0E-02
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 90 1 0.12 4 3.2E-02
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 0.12 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 0.12 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 0.12 0 0
CUI: C4225179
Disease: COWDEN SYNDROME 7
COWDEN SYNDROME 7 		1 0 1 0.12 0 0
CUI: C0040127
Disease: Thyroid Crisis
Thyroid Crisis 		2 0 1 0.11 0 0
CUI: C1863340
Disease: PITUITARY ADENOMA PREDISPOSITION (disorder)
PITUITARY ADENOMA PREDISPOSITION (disorder) 		2 0 1 0.11 0 0
CUI: C2931210
Disease: Usher syndrome, type 1F
Usher syndrome, type 1F 		2 1 1 0.11 1 2.5E-02
CUI: C3150654
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84A
DEAFNESS, AUTOSOMAL RECESSIVE 84A 		2 3 1 0.11 1 2.4E-02
CUI: C3539888
Disease: ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3 		2 0 1 0.11 0 0
CUI: C3552574
Disease: HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA 		2 0 1 0.11 0 0
CUI: C3809672
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37 		2 0 1 0.11 0 0
CUI: C4021725
Disease: Reduced activity of N-acetylglucosaminyltransferase II
Reduced activity of N-acetylglucosaminyltransferase II 		2 0 1 0.11 0 0
CUI: C4025624
Disease: Endopolyploidy on chromosome studies of bone marrow
Endopolyploidy on chromosome studies of bone marrow 		2 0 1 0.11 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 3 0.11 2 9.7E-03
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 2 0.11 0 0
CUI: C0015382
Disease: Extraversion (Psychology)
Extraversion (Psychology) 		3 0 1 1.0E-01 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 2 1.0E-01 0 0