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: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy 		7 0 5 0.42 0 0
CUI: C0205882
Disease: Infections, Parvovirus
Infections, Parvovirus 		12 0 5 0.29 0 0
CUI: C0152109
Disease: Juvenile Spinal Muscular Atrophy
Juvenile Spinal Muscular Atrophy 		14 0 5 0.26 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		15 0 5 0.25 0 0
CUI: C0037933
Disease: Spinal Diseases
Spinal Diseases 		16 0 5 0.24 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy 		16 0 5 0.24 0 0
CUI: C4750288
Disease: Spinal muscular atrophy with lower extremity predominance
Spinal muscular atrophy with lower extremity predominance 		6 0 3 0.23 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 5 0.22 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 5 0.22 0 0
CUI: C0026821
Disease: Muscle Cramp
Muscle Cramp 		26 0 6 0.20 0 0
CUI: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 2 0.20 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 2 0.20 0 0
CUI: C1511934
Disease: Differentiating Neuroblastoma
Differentiating Neuroblastoma 		20 0 5 0.20 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 2 0.20 0 0
CUI: C4732793
Disease: Polyminimyoclonus
Polyminimyoclonus 		2 0 2 0.20 0 0
CUI: C0155141
Disease: Acute conjunctivitis
Acute conjunctivitis 		3 0 2 0.18 0 0
CUI: C0393546
Disease: Oculopharyngeal Spinal Muscular Atrophy
Oculopharyngeal Spinal Muscular Atrophy 		3 0 2 0.18 0 0
CUI: C0751334
Disease: Progressive Proximal Myelopathic Muscular Atrophy
Progressive Proximal Myelopathic Muscular Atrophy 		3 0 2 0.18 0 0
CUI: C0751335
Disease: Scapuloperoneal Form of Spinal Muscular Atrophy
Scapuloperoneal Form of Spinal Muscular Atrophy 		3 0 2 0.18 0 0
CUI: C1301959
Disease: Bulbar weakness
Bulbar weakness 		3 0 2 0.18 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 2 0.18 0 0
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		3 0 2 0.18 0 0
CUI: C4024911
Disease: Acute infantile spinal muscular atrophy
Acute infantile spinal muscular atrophy 		3 0 2 0.18 0 0
CUI: C0270764
Disease: Motor Neuron Disease, Lower
Motor Neuron Disease, Lower 		23 0 5 0.18 0 0
CUI: C1864497
Disease: PSORIASIS 2
PSORIASIS 2 		4 0 2 0.17 0 0