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: C0009084
Disease: Cluster A personality disorder
Cluster A personality disorder 		1 0 1 3.8E-02 0 0
CUI: C0036339
Disease: Schizoid Personality Disorder
Schizoid Personality Disorder 		1 0 1 3.8E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 3.8E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 3.8E-02 0 0
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		1 0 1 3.8E-02 0 0
CUI: C0338777
Disease: Opium Dependence
Opium Dependence 		1 0 1 3.8E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 3.8E-02 0 0
CUI: C0497219
Disease: Hearing complaints (excluding H84-86)
Hearing complaints (excluding H84-86) 		1 0 1 3.8E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 3.8E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.8E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 3.8E-02 0 0
CUI: C0856561
Disease: Opium addiction
Opium addiction 		1 0 1 3.8E-02 0 0
CUI: C0919582
Disease: Sudden onset of sleep
Sudden onset of sleep 		1 0 1 3.8E-02 0 0
CUI: C1112173
Disease: Transient psychosis
Transient psychosis 		1 0 1 3.8E-02 0 0
CUI: C1536087
Disease: Negative myoclonus
Negative myoclonus 		1 0 1 3.8E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 3.8E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 3.8E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 3.8E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 3.8E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 3.8E-02 0 0
CUI: C1840347
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder) 		1 0 1 3.8E-02 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 3.8E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 3.8E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 0 1 3.8E-02 0 0
CUI: C1865818
Disease: DYSTONIA 7, TORSION (disorder)
DYSTONIA 7, TORSION (disorder) 		1 0 1 3.8E-02 0 0