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: C4016684
Disease: MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL DOMINANT
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY, AUTOSOMAL DOMINANT 		1 0 1 0.12 0 0
CUI: C4016724
Disease: RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE
RIPPLING MUSCLE DISEASE 2, AUTOSOMAL RECESSIVE 		1 0 1 0.12 0 0
CUI: C4017156
Disease: MCARDLE DISEASE, MILD
MCARDLE DISEASE, MILD 		1 0 1 0.12 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 0.12 0 0
CUI: C4732750
Disease: Decreased hemoglobin concentration
Decreased hemoglobin concentration 		1 0 1 0.12 0 0
CUI: C4749335
Disease: Rippling muscle disease with myasthenia gravis
Rippling muscle disease with myasthenia gravis 		1 0 1 0.12 0 0
CUI: C4751434
Disease: Isolated asymptomatic elevation of creatine phosphokinase
Isolated asymptomatic elevation of creatine phosphokinase 		1 0 1 0.12 0 0
CUI: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		2 0 1 0.11 0 0
CUI: C0039223
Disease: Tabes Dorsalis
Tabes Dorsalis 		2 0 1 0.11 0 0
CUI: C0241705
Disease: Difficulty passing urine
Difficulty passing urine 		2 0 1 0.11 0 0
CUI: C0262918
Disease: Extraocular Muscle Paresis
Extraocular Muscle Paresis 		2 0 1 0.11 0 0
CUI: C0268149
Disease: Glycogen storage disease type X
Glycogen storage disease type X 		2 0 1 0.11 0 0
CUI: C0546466
Disease: Idiopathic cardiac hypertrophy
Idiopathic cardiac hypertrophy 		2 0 1 0.11 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 1 0.11 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure 		2 0 1 0.11 0 0
CUI: C1832560
Disease: RIPPLING MUSCLE DISEASE 2 (disorder)
RIPPLING MUSCLE DISEASE 2 (disorder) 		2 0 1 0.11 0 0
CUI: C1838254
Disease: RIPPLING MUSCLE DISEASE 1
RIPPLING MUSCLE DISEASE 1 		2 0 1 0.11 0 0
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 1 0.11 0 0
CUI: C1845861
Disease: MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT
MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT 		2 0 1 0.11 0 0
CUI: C3279093
Disease: LONG QT SYNDROME 2/9, DIGENIC
LONG QT SYNDROME 2/9, DIGENIC 		2 0 1 0.11 0 0
CUI: C3280443
Disease: MYOPATHY, DISTAL, TATEYAMA TYPE
MYOPATHY, DISTAL, TATEYAMA TYPE 		2 0 1 0.11 0 0
CUI: C3805450
Disease: Calf muscle hypoplasia
Calf muscle hypoplasia 		2 0 1 0.11 0 0
CUI: C4022546
Disease: Reduced erythrocyte 2,3-diphosphoglycerate concentration
Reduced erythrocyte 2,3-diphosphoglycerate concentration 		2 0 1 0.11 0 0
CUI: C4022653
Disease: Abnormal muscle fiber protein expression
Abnormal muscle fiber protein expression 		2 0 1 0.11 0 0
CUI: C4280804
Disease: Percussion-induced rapid rolling muscle contractions
Percussion-induced rapid rolling muscle contractions 		2 0 1 0.11 0 0