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: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 1.0E-01 0 0
CUI: C0521723
Disease: Corneal dystrophy, epithelial basement membrane
Corneal dystrophy, epithelial basement membrane 		1 0 1 1.0E-01 0 0
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		1 0 1 1.0E-01 0 0
CUI: C1262008
Disease: Hyperphosphatasemia
Hyperphosphatasemia 		1 0 1 1.0E-01 0 0
CUI: C1266055
Disease: Mixed medullary-follicular carcinoma
Mixed medullary-follicular carcinoma 		1 0 1 1.0E-01 0 0
CUI: C1266099
Disease: Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation
Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation 		1 0 1 1.0E-01 0 0
CUI: C1608983
Disease: Mal de debarquement
Mal de debarquement 		1 0 1 1.0E-01 0 0
CUI: C1641846
Disease: Groenouw corneal dystrophy type I (disorder)
Groenouw corneal dystrophy type I (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1709166
Disease: Neoplastic C-Cell Hyperplasia
Neoplastic C-Cell Hyperplasia 		1 0 1 1.0E-01 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 1 1 1.0E-01 1 2.7E-02
CUI: C1837974
Disease: Corneal Dystrophy, Lattice Type IIIA
Corneal Dystrophy, Lattice Type IIIA 		1 0 1 1.0E-01 0 0
CUI: C1865323
Disease: Migraine, Familial Basilar
Migraine, Familial Basilar 		1 1 1 1.0E-01 1 2.7E-02
CUI: C2349460
Disease: Pure menstrual migraine
Pure menstrual migraine 		1 0 1 1.0E-01 0 0
CUI: C3150908
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13 		1 0 1 1.0E-01 0 0
CUI: C3264000
Disease: Refractory juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy 		1 0 1 1.0E-01 0 0
CUI: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 1.0E-01 0 0
CUI: C3827273
Disease: Sudden Unexplained Death in Childhood
Sudden Unexplained Death in Childhood 		1 0 1 1.0E-01 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 1.0E-01 0 0
CUI: C4021060
Disease: Hyperplastic labia majora
Hyperplastic labia majora 		1 0 1 1.0E-01 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 1.0E-01 0 0
CUI: C4022872
Disease: Reduced thyroxin-binding globulin
Reduced thyroxin-binding globulin 		1 0 1 1.0E-01 0 0
CUI: C4024792
Disease: Nodular corneal dystrophy
Nodular corneal dystrophy 		1 0 1 1.0E-01 0 0
CUI: C4024796
Disease: Punctate corneal dystrophy
Punctate corneal dystrophy 		1 0 1 1.0E-01 0 0
CUI: C4280709
Disease: Impaired neutrophil chemotaxis
Impaired neutrophil chemotaxis 		1 0 1 1.0E-01 0 0
CUI: C4310716
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42 		1 28 1 1.0E-01 5 8.3E-02