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: C0231531
Disease: Muscle fibrillation
Muscle fibrillation 		8 0 5 0.10 0 0
CUI: C4025785
Disease: Abnormality of the foot musculature
Abnormality of the foot musculature 		8 0 5 0.10 0 0
CUI: C1836599
Disease: Macrocephaly at birth
Macrocephaly at birth 		12 0 5 9.6E-02 0 0
CUI: C0235820
Disease: Neonatal encephalopathy
Neonatal encephalopathy 		26 0 6 9.2E-02 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 5 8.9E-02 0 0
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		74 0 9 8.2E-02 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 5 8.1E-02 0 0
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous 		36 0 6 8.0E-02 0 0
CUI: C0263218
Disease: Pyogenic granuloma of skin
Pyogenic granuloma of skin 		10 0 4 7.8E-02 0 0
CUI: C1856694
Disease: Areflexia of lower limbs
Areflexia of lower limbs 		24 0 5 7.8E-02 0 0
CUI: C1842170
Disease: Centrally nucleated skeletal muscle fibers
Centrally nucleated skeletal muscle fibers 		25 0 5 7.7E-02 0 0
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I 		11 0 4 7.7E-02 0 0
CUI: C0085653
Disease: Pyogenic granuloma
Pyogenic granuloma 		13 0 4 7.4E-02 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 4 7.4E-02 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 4 7.4E-02 0 0
CUI: C4721772
Disease: Postoperative delirium
Postoperative delirium 		42 0 6 7.4E-02 0 0
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
Acute appendicitis NOS (disorder) 		43 0 6 7.3E-02 0 0
CUI: C1848395
Disease: Large for gestational age
Large for gestational age 		43 0 6 7.3E-02 0 0
CUI: C0231230
Disease: Fatigability
Fatigability 		29 0 5 7.2E-02 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 5 7.2E-02 0 0
CUI: C0011263
Disease: Multi-infarct dementia
Multi-infarct dementia 		30 0 5 7.1E-02 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 5 7.1E-02 0 0
CUI: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 4 7.0E-02 0 0
CUI: C0014733
Disease: Erysipelas
Erysipelas 		17 0 4 6.9E-02 0 0
CUI: C1367536
Disease: Nasopharyngeal Angiofibroma
Nasopharyngeal Angiofibroma 		17 0 4 6.9E-02 0 0