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: C3554447
Disease: DYSTONIA 25
DYSTONIA 25 		2 0 2 0.12 0 0
CUI: C4025151
Disease: Increased bone density with cystic changes
Increased bone density with cystic changes 		2 0 2 0.12 0 0
CUI: C4025515
Disease: Cortical subperiosteal resorption of humeral metaphyses
Cortical subperiosteal resorption of humeral metaphyses 		2 0 2 0.12 0 0
CUI: C0949445
Disease: Cervical Dystonia
Cervical Dystonia 		23 0 4 0.11 0 0
CUI: C1864105
Disease: Low urinary cyclic AMP response to PTH administration
Low urinary cyclic AMP response to PTH administration 		3 0 2 0.11 0 0
CUI: C2242577
Disease: Oromandibular dystonia
Oromandibular dystonia 		13 0 3 0.11 0 0
CUI: C2875058
Disease: Familial torsion dystonia
Familial torsion dystonia 		3 0 2 0.11 0 0
CUI: C3887667
Disease: Retrocollis
Retrocollis 		3 0 2 0.11 0 0
CUI: C0266006
Disease: Pili torti-deafness syndrome
Pili torti-deafness syndrome 		14 0 3 0.11 0 0
CUI: C0151940
Disease: Hypocalcemic tetany
Hypocalcemic tetany 		4 0 2 0.11 0 0
CUI: C0342198
Disease: Thyrotoxicosis due to pituitary thyroid hormone resistance
Thyrotoxicosis due to pituitary thyroid hormone resistance 		4 0 2 0.11 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia 		4 0 2 0.11 0 0
CUI: C3697670
Disease: Spinal cord myoclonus
Spinal cord myoclonus 		4 0 2 0.11 0 0
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements 		37 0 5 0.10 0 0
CUI: C1851945
Disease: DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT 		5 0 2 1.0E-01 0 0
CUI: C4551853
Disease: Diaphyseal sclerosis
Diaphyseal sclerosis 		6 0 2 9.5E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 3 9.1E-02 0 0
CUI: C1834570
Disease: Myoclonic dystonia
Myoclonic dystonia 		19 0 3 9.1E-02 0 0
CUI: C0005747
Disease: Blepharospasm
Blepharospasm 		44 0 5 8.9E-02 0 0
CUI: C1867138
Disease: Upper limb postural tremor
Upper limb postural tremor 		8 0 2 8.7E-02 0 0
CUI: C2932715
Disease: Pseudohypoparathyroidism Type 1B
Pseudohypoparathyroidism Type 1B 		8 0 2 8.7E-02 0 0
CUI: C0154676
Disease: Organic writer's cramp
Organic writer's cramp 		9 0 2 8.3E-02 0 0
CUI: C1868681
Disease: DYSTONIA 12
DYSTONIA 12 		9 0 2 8.3E-02 0 0
CUI: C1449843
Disease: Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I, Autosomal Recessive 		10 0 2 8.0E-02 0 0
CUI: C2713447
Disease: Hyperpotassemia and Hypertension, Familial
Hyperpotassemia and Hypertension, Familial 		10 0 2 8.0E-02 0 0