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: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases 		1 0 1 1.7E-02 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 1.7E-02 0 0
CUI: C0334483
Disease: Adult rhabdomyoma
Adult rhabdomyoma 		1 0 1 1.7E-02 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 1.7E-02 0 0
CUI: C0581375
Disease: Double coronary vessel disease
Double coronary vessel disease 		1 0 1 1.7E-02 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated 		1 0 1 1.7E-02 0 0
CUI: C0857256
Disease: Unwell
Unwell 		1 0 1 1.7E-02 0 0
CUI: C0858233
Disease: Stridor, Congenital
Stridor, Congenital 		1 0 1 1.7E-02 0 0
CUI: C1142081
Disease: Chronic lymphocytic leukaemia transformation
Chronic lymphocytic leukaemia transformation 		1 0 1 1.7E-02 0 0
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity 		1 0 1 1.7E-02 0 0
CUI: C1275303
Disease: Erythrodermic mycosis fungoides
Erythrodermic mycosis fungoides 		1 0 1 1.7E-02 0 0
CUI: C1392046
Disease: Cardiovascular insufficiency
Cardiovascular insufficiency 		1 0 1 1.7E-02 0 0
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		1 0 1 1.7E-02 0 0
CUI: C1836076
Disease: Amyotrophic Lateral Sclerosis, Chmp2B-Related
Amyotrophic Lateral Sclerosis, Chmp2B-Related 		1 0 1 1.7E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 1.7E-02 0 0
CUI: C1842026
Disease: GLAUCOMA 1, OPEN ANGLE, E
GLAUCOMA 1, OPEN ANGLE, E 		1 0 1 1.7E-02 0 0
CUI: C1843315
Disease: Neuronopathy, Distal Hereditary Motor, Type Viib
Neuronopathy, Distal Hereditary Motor, Type Viib 		1 0 1 1.7E-02 0 0
CUI: C1853154
Disease: Nemaline Myopathy 7
Nemaline Myopathy 7 		1 0 1 1.7E-02 0 0
CUI: C1853949
Disease: MYASTHENIA, FAMILIAL INFANTILE, 1
MYASTHENIA, FAMILIAL INFANTILE, 1 		1 0 1 1.7E-02 0 0
CUI: C1854058
Disease: SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE
SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE 		1 0 1 1.7E-02 0 0
CUI: C1854059
Disease: AMYOTROPHIC LATERAL SCLEROSIS, TYPICAL
AMYOTROPHIC LATERAL SCLEROSIS, TYPICAL 		1 0 1 1.7E-02 0 0
CUI: C1855000
Disease: Agenesis of central incisor
Agenesis of central incisor 		1 0 1 1.7E-02 0 0
CUI: C1858154
Disease: CARDIOMYOPATHY, DILATED, 1I
CARDIOMYOPATHY, DILATED, 1I 		1 0 1 1.7E-02 0 0
CUI: C1858891
Disease: PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS 		1 0 1 1.7E-02 0 0
CUI: C1866077
Disease: MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5 		1 0 1 1.7E-02 0 0