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: C1840365
Disease: King Denborough syndrome
King Denborough syndrome
1 0 1 1.00 0 0
Multiminicore Disease, Moderate, with Hand Involvement
1 0 1 1.00 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy
1 0 1 1.00 0 0
Malignant hyperthermia susceptibility type 1
1 0 1 1.00 0 0
CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
1 0 1 1.00 0 0
CUI: C4476998
Disease: Frog-leg posture
Frog-leg posture
1 0 1 1.00 0 0
Congenital myopathy with myasthenic-like onset
1 0 1 1.00 0 0
Benign Samaritan congenital myopathy
1 0 1 1.00 0 0
CUI: C0155338
Disease: Total ophthalmoplegia
Total ophthalmoplegia
2 0 1 0.50 0 0
Exertional rhabdomyolysis (disorder)
2 0 1 0.50 0 0
Central core regions in muscle fibers
2 0 1 0.50 0 0
Type 1 and type 2 muscle fiber minicore regions
2 0 1 0.50 0 0
CUI: C4073214
Disease: Abnormality of masseter muscle
Abnormality of masseter muscle
2 0 1 0.50 0 0
Cardiomyocyte mitochondrial proliferation
2 0 1 0.50 0 0
CUI: C0333759
Disease: Muscle fiber hypertrophy
Muscle fiber hypertrophy
3 0 1 0.33 0 0
High-output congestive heart failure
3 0 1 0.33 0 0
CUI: C3267178
Disease: Axial myopathy
Axial myopathy
3 0 1 0.33 0 0
CUI: C4023067
Disease: Sternocleidomastoid amyotrophy
Sternocleidomastoid amyotrophy
3 0 1 0.33 0 0
CUI: C4023104
Disease: Intermittent painful muscle spasms
Intermittent painful muscle spasms
3 0 1 0.33 0 0
CUI: C4023375
Disease: Tibialis atrophy
Tibialis atrophy
3 0 1 0.33 0 0
Internally nucleated skeletal muscle fibers
3 0 1 0.33 0 0
Mixed respiratory and metabolic acidosis
4 0 1 0.25 0 0
CUI: C1855126
Disease: 3-Methylglutaconic Aciduria Type IV
3-Methylglutaconic Aciduria Type IV
4 0 1 0.25 0 0
Non-sustained ventricular tachycardia
5 0 1 0.20 0 0
CUI: C1260922
Disease: Abnormal breathing
Abnormal breathing
5 0 1 0.20 0 0