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: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 6.7E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 6.7E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 6.7E-02 0 0
CUI: C0149877
Disease: Hypoglycemic encephalopathy
Hypoglycemic encephalopathy 		1 0 1 6.7E-02 0 0
CUI: C0238391
Disease: PRIMARY LACTIC ACIDOSIS
PRIMARY LACTIC ACIDOSIS 		1 0 1 6.7E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 6.7E-02 0 0
CUI: C0267430
Disease: Noninfectious colitis
Noninfectious colitis 		1 0 1 6.7E-02 0 0
CUI: C0342970
Disease: Increased oxygen demand
Increased oxygen demand 		1 0 1 6.7E-02 0 0
CUI: C0345903
Disease: Anal skin tag
Anal skin tag 		1 0 1 6.7E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 6.7E-02 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 6.7E-02 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 6.7E-02 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 6.7E-02 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 6.7E-02 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 6.7E-02 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 6.7E-02 0 0
CUI: C0857576
Disease: Abnormality of thyroid physiology
Abnormality of thyroid physiology 		1 0 1 6.7E-02 0 0
CUI: C1321275
Disease: Non-specific colitis
Non-specific colitis 		1 0 1 6.7E-02 0 0
CUI: C1332259
Disease: Adenocarcinoma of anal canal
Adenocarcinoma of anal canal 		1 0 1 6.7E-02 0 0
CUI: C1333084
Disease: Colon Neuroendocrine Tumor G1
Colon Neuroendocrine Tumor G1 		1 0 1 6.7E-02 0 0
CUI: C1333110
Disease: Colorectal High Grade Intraepithelial Neoplasia
Colorectal High Grade Intraepithelial Neoplasia 		1 0 1 6.7E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 6.7E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 6.7E-02 0 0
CUI: C1533587
Disease: Hydroxymethylglutaric aciduria
Hydroxymethylglutaric aciduria 		1 0 1 6.7E-02 0 0
CUI: C1837257
Disease: Lipid accumulation in hepatocytes
Lipid accumulation in hepatocytes 		1 0 1 6.7E-02 0 0