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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 2.0E-02 0 0
CUI: C0017162
Disease: Gastroenteritis, Transmissible, of Swine
Gastroenteritis, Transmissible, of Swine 		1 0 1 2.0E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.0E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 2.0E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 2.0E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 2.0E-02 0 0
CUI: C0451669
Disease: Neuropathy in association with hereditary ataxia
Neuropathy in association with hereditary ataxia 		1 0 1 2.0E-02 0 0
CUI: C0497219
Disease: Hearing complaints (excluding H84-86)
Hearing complaints (excluding H84-86) 		1 0 1 2.0E-02 0 0
CUI: C0524679
Disease: Neuropapillitis
Neuropapillitis 		1 0 1 2.0E-02 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 2.0E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 2.0E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 2.0E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 2.0E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.0E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 2.0E-02 0 0
CUI: C0850629
Disease: radiating back pain
radiating back pain 		1 0 1 2.0E-02 0 0
CUI: C1333422
Disease: epithelioid cell intraocular melanoma
epithelioid cell intraocular melanoma 		1 0 1 2.0E-02 0 0
CUI: C1335484
Disease: Gastric T-Cell Non-Hodgkin Lymphoma
Gastric T-Cell Non-Hodgkin Lymphoma 		1 0 1 2.0E-02 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome 		1 0 1 2.0E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.0E-02 0 0
CUI: C1833373
Disease: Inclusion Body Myopathy, Autosomal Recessive
Inclusion Body Myopathy, Autosomal Recessive 		1 0 1 2.0E-02 0 0
CUI: C1834692
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA 		1 0 1 2.0E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 2.0E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 2.0E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 2.0E-02 0 0