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: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia 		9 0 2 1.0E-01 0 0
CUI: C0752197
Disease: Adult-Onset Dystonias
Adult-Onset Dystonias 		9 0 2 1.0E-01 0 0
CUI: C3888090
Disease: Early onset torsion dystonia
Early onset torsion dystonia 		22 0 3 9.4E-02 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder 		11 0 2 9.1E-02 0 0
CUI: C0949445
Disease: Cervical Dystonia
Cervical Dystonia 		23 0 3 9.1E-02 0 0
CUI: C0231698
Disease: Gait, Scissors
Gait, Scissors 		12 0 2 8.7E-02 0 0
CUI: C0231471
Disease: Abnormal posture
Abnormal posture 		13 0 2 8.3E-02 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 4 8.2E-02 0 0
CUI: C0240116
Disease: Hyperactive patellar reflex
Hyperactive patellar reflex 		14 0 2 8.0E-02 0 0
CUI: C0266006
Disease: Pili torti-deafness syndrome
Pili torti-deafness syndrome 		14 0 2 8.0E-02 0 0
CUI: C0040485
Disease: Torticollis
Torticollis 		55 0 5 7.9E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 7.7E-02 0 0
CUI: C0393577
Disease: Pallidal degeneration
Pallidal degeneration 		1 0 1 7.7E-02 0 0
CUI: C0454601
Disease: Pyramidal dysarthria
Pyramidal dysarthria 		1 0 1 7.7E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 7.7E-02 0 0
CUI: C0747733
Disease: Polychondritis
Polychondritis 		1 0 1 7.7E-02 0 0
CUI: C1333446
Disease: Esophageal Gastrointestinal Stromal Tumor
Esophageal Gastrointestinal Stromal Tumor 		1 0 1 7.7E-02 0 0
CUI: C1378512
Disease: Blast cell leukemia
Blast cell leukemia 		1 0 1 7.7E-02 0 0
CUI: C1839564
Disease: Jensen syndrome
Jensen syndrome 		1 0 1 7.7E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 0 1 7.7E-02 0 0
CUI: C2676281
Disease: DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (disorder)
DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 7.7E-02 0 0
CUI: C2680446
Disease: SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE 		1 0 1 7.7E-02 0 0
CUI: C2751506
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL 		1 0 1 7.7E-02 0 0
CUI: C2937300
Disease: Congenital hereditary muscular dystrophy
Congenital hereditary muscular dystrophy 		1 0 1 7.7E-02 0 0
CUI: C2938912
Disease: Hyperintensity of cerebral white matter on MRI
Hyperintensity of cerebral white matter on MRI 		15 0 2 7.7E-02 0 0