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: C1833021
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6
DEAFNESS, AUTOSOMAL DOMINANT 6 		1 11 1 1.00 1 8.3E-02
CUI: C1857288
Disease: Limited mobility of proximal interphalangeal joint
Limited mobility of proximal interphalangeal joint 		1 0 1 1.00 0 0
CUI: C3280358
Disease: Wolfram-Like Syndrome, Autosomal Dominant
Wolfram-Like Syndrome, Autosomal Dominant 		1 5 1 1.00 2 0.40
CUI: C3544080
Disease: Congenital central diabetes insipidus
Congenital central diabetes insipidus 		1 0 1 1.00 0 0
CUI: C3805412
Disease: CATARACT 41
CATARACT 41 		1 0 1 1.00 0 0
CUI: C3810445
Disease: Low-frequency sensorineural hearing impairment
Low-frequency sensorineural hearing impairment 		1 0 1 1.00 0 0
CUI: C0348932
Disease: Other specified diabetes mellitus with unspecified complications
Other specified diabetes mellitus with unspecified complications 		2 0 1 0.50 0 0
CUI: C1846464
Disease: Globe retraction and deviation on adduction
Globe retraction and deviation on adduction 		2 0 1 0.50 0 0
CUI: C4293672
Disease: Abnormality of mesentery morphology
Abnormality of mesentery morphology 		3 0 1 0.33 0 0
CUI: C0235280
Disease: Ototoxicity
Ototoxicity 		4 0 1 0.25 0 0
CUI: C0271972
Disease: Thiamine-responsive megaloblastic anemia
Thiamine-responsive megaloblastic anemia 		4 0 1 0.25 0 0
CUI: C1852282
Disease: DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder) 		4 0 1 0.25 0 0
CUI: C3826233
Disease: Hearing impaired children
Hearing impaired children 		4 0 1 0.25 0 0
CUI: C4023641
Disease: Abnormality of the upper urinary tract
Abnormality of the upper urinary tract 		4 0 1 0.25 0 0
CUI: C0748061
Disease: psychiatric hospitalization
psychiatric hospitalization 		5 0 1 0.20 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 0 1 0.14 0 0
CUI: C1858028
Disease: WOLFRAM SYNDROME 2
WOLFRAM SYNDROME 2 		7 0 1 0.14 0 0
CUI: C1562061
Disease: Microspherophakia
Microspherophakia 		9 0 1 0.11 0 0
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		9 0 1 0.11 0 0
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm 		12 0 1 8.3E-02 0 0
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine 		12 0 1 8.3E-02 0 0
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 1 6.7E-02 0 0
CUI: C0005122
Disease: Beriberi
Beriberi 		16 0 1 6.2E-02 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration 		16 0 1 6.2E-02 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 1 6.2E-02 0 0