Source: CLINVAR ×
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: C0426421
Disease: Wide nose
Wide nose 		1 0 1 9.7E-03 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 0 1 9.7E-03 0 0
CUI: C0432355
Disease: Hypoplasia of nipple
Hypoplasia of nipple 		1 0 1 9.7E-03 0 0
CUI: C0549423
Disease: Obstructive Hydrocephalus
Obstructive Hydrocephalus 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		1 0 1 9.7E-03 0 0
CUI: C0677861
Disease: Bilateral Malignant Neoplasm
Bilateral Malignant Neoplasm 		1 1 1 9.7E-03 1 7.6E-03
CUI: C0751587
Disease: CADASIL Syndrome
CADASIL Syndrome 		1 0 1 9.7E-03 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		1 9 1 9.7E-03 1 7.2E-03
CUI: C0795888
Disease: AUTISM, SUSCEPTIBILITY TO, X-LINKED 4
AUTISM, SUSCEPTIBILITY TO, X-LINKED 4 		1 0 1 9.7E-03 0 0
CUI: C0795934
Disease: Digitorenocerebral Syndrome
Digitorenocerebral Syndrome 		1 11 1 9.7E-03 8 6.0E-02
CUI: C0855389
Disease: Renin decreased
Renin decreased 		1 0 1 9.7E-03 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile 		1 0 1 9.7E-03 0 0
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia 		1 2 1 9.7E-03 1 7.6E-03
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		1 0 1 9.7E-03 0 0
CUI: C1291230
Disease: 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3-Hydroxyacyl-CoA Dehydrogenase Deficiency 		1 0 1 9.7E-03 0 0
CUI: C1332262
Disease: Anal canal squamous cell carcinoma
Anal canal squamous cell carcinoma 		1 0 1 9.7E-03 0 0
CUI: C1332549
Disease: Bilateral Carcinoma
Bilateral Carcinoma 		1 1 1 9.7E-03 1 7.6E-03
CUI: C1387925
Disease: Abnormality of limbs
Abnormality of limbs 		1 1 1 9.7E-03 1 7.6E-03
CUI: C1419610
Disease: RP23 gene
RP23 gene 		1 0 1 9.7E-03 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		1 108 1 9.7E-03 1 4.2E-03
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		1 48 1 9.7E-03 1 5.6E-03
CUI: C1832127
Disease: Square face
Square face 		1 0 1 9.7E-03 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 9.7E-03 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		1 0 1 9.7E-03 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 9.7E-03 0 0