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: C0152109
Disease: Juvenile Spinal Muscular Atrophy
Juvenile Spinal Muscular Atrophy 		14 17 10 0.26 1 4.2E-02
CUI: C4304411
Disease: Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum and Cockayne syndrome complex 		10 0 7 0.19 0 0
CUI: C0700595
Disease: Spinal Muscular Atrophies of Childhood
Spinal Muscular Atrophies of Childhood 		6 0 6 0.18 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 7 0.17 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy 		16 0 7 0.16 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 7 0.16 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 7 0.15 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		15 0 6 0.14 0 0
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy 		7 0 5 0.14 0 0
CUI: C0878555
Disease: Diffuse panbronchiolitis
Diffuse panbronchiolitis 		26 0 7 0.13 0 0
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy 		10 0 5 0.13 0 0
CUI: C0205882
Disease: Infections, Parvovirus
Infections, Parvovirus 		12 0 5 0.12 0 0
CUI: C0270764
Disease: Motor Neuron Disease, Lower
Motor Neuron Disease, Lower 		23 0 6 0.12 0 0
CUI: C2931358
Disease: Muscular atrophy, spinal, infantile chronic form
Muscular atrophy, spinal, infantile chronic form 		4 0 4 0.12 0 0
CUI: C1955934
Disease: Trichothiodystrophy Syndromes
Trichothiodystrophy Syndromes 		33 0 7 0.12 0 0
CUI: C1843505
Disease: Degeneration of anterior horn cells
Degeneration of anterior horn cells 		15 0 5 0.11 0 0
CUI: C0037933
Disease: Spinal Diseases
Spinal Diseases 		16 0 5 0.11 0 0
CUI: C0393538
Disease: Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type II 		6 9 4 0.11 2 0.13
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 8 0.11 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 4 0.11 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 5 0.11 0 0
CUI: C1511934
Disease: Differentiating Neuroblastoma
Differentiating Neuroblastoma 		20 0 5 0.10 0 0
CUI: C0035613
Disease: Rift Valley Fever
Rift Valley Fever 		45 0 7 9.7E-02 0 0
CUI: C0878787
Disease: Growth failure
Growth failure 		84 0 10 9.3E-02 0 0
CUI: C0026821
Disease: Muscle Cramp
Muscle Cramp 		26 0 5 9.1E-02 0 0