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: C3715156
Disease: AMYOTROPHIC LATERAL SCLEROSIS 20
AMYOTROPHIC LATERAL SCLEROSIS 20 		2 0 2 6.1E-02 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 3 6.0E-02 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 3 5.9E-02 0 0
CUI: C4021165
Disease: Abnormality of long bone morphology
Abnormality of long bone morphology 		3 0 2 5.9E-02 0 0
CUI: C4022588
Disease: Fatigable weakness of swallowing muscles
Fatigable weakness of swallowing muscles 		39 0 4 5.9E-02 0 0
CUI: C4023052
Disease: Ubiquitin-positive cerebral inclusion bodies
Ubiquitin-positive cerebral inclusion bodies 		3 0 2 5.9E-02 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 4 5.8E-02 0 0
CUI: C0577573
Disease: Mass of body region
Mass of body region 		22 0 3 5.8E-02 0 0
CUI: C1516061
Disease: Astler-Coller B1 Rectal Carcinoma
Astler-Coller B1 Rectal Carcinoma 		22 0 3 5.8E-02 0 0
CUI: C0343187
Disease: Primary systemic vasculitis
Primary systemic vasculitis 		4 0 2 5.7E-02 0 0
CUI: C1834014
Disease: Oculopharyngodistal Myopathy
Oculopharyngodistal Myopathy 		4 0 2 5.7E-02 0 0
CUI: C4025347
Disease: Weakness of muscles of respiration
Weakness of muscles of respiration 		4 0 2 5.7E-02 0 0
CUI: C0749163
Disease: Supraglottic Squamous Cell Carcinoma
Supraglottic Squamous Cell Carcinoma 		5 0 2 5.6E-02 0 0
CUI: C1392224
Disease: Centrocytic lymphoma
Centrocytic lymphoma 		5 0 2 5.6E-02 0 0
CUI: C1563705
Disease: Nephrogenic Diabetes Insipidus, Type I
Nephrogenic Diabetes Insipidus, Type I 		24 0 3 5.6E-02 0 0
CUI: C4324298
Disease: Tumour inflammation
Tumour inflammation 		24 0 3 5.6E-02 0 0
CUI: C0343755
Disease: HIV Wasting Syndrome
HIV Wasting Syndrome 		6 0 2 5.4E-02 0 0
CUI: C3826604
Disease: Celiac disease in children
Celiac disease in children 		6 0 2 5.4E-02 0 0
CUI: C3898147
Disease: Neonatal Hypoxic Ischemic Encephalopathy
Neonatal Hypoxic Ischemic Encephalopathy 		26 0 3 5.4E-02 0 0
CUI: C0005944
Disease: Metabolic Bone Disorder
Metabolic Bone Disorder 		66 0 5 5.3E-02 0 0
CUI: C0749870
Disease: Upper motor neuron signs
Upper motor neuron signs 		7 0 2 5.3E-02 0 0
CUI: C0860197
Disease: Advanced chronic liver disease
Advanced chronic liver disease 		7 0 2 5.3E-02 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		7 0 2 5.3E-02 0 0
CUI: C0522224
Disease: Paralysed
Paralysed 		68 0 5 5.2E-02 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 4 5.2E-02 0 0