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: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		34 0 3 4.8E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 4 4.8E-02 0 0
CUI: C0033790
Disease: Pseudobulbar Palsy
Pseudobulbar Palsy 		13 0 2 4.8E-02 0 0
CUI: C0344917
Disease: Left ventricular outflow tract obstruction
Left ventricular outflow tract obstruction 		13 0 2 4.8E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 2 4.8E-02 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 3 4.8E-02 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 4 4.6E-02 0 0
CUI: C0278584
Disease: Metastatic Carcinoma to the Uterine Cervix
Metastatic Carcinoma to the Uterine Cervix 		15 0 2 4.5E-02 0 0
CUI: C0854193
Disease: Cognitive deterioration
Cognitive deterioration 		39 0 3 4.5E-02 0 0
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy 		16 0 2 4.4E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 2 4.3E-02 0 0
CUI: C0522224
Disease: Paralysed
Paralysed 		68 0 4 4.2E-02 0 0
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum 		45 0 3 4.1E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 0 3 4.1E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 2 4.0E-02 0 0
CUI: C1096249
Disease: Calcification of the aorta
Calcification of the aorta 		21 0 2 4.0E-02 0 0
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		21 0 2 4.0E-02 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 2 4.0E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		22 0 2 3.9E-02 0 0
CUI: C0030794
Disease: Pelvic Pain
Pelvic Pain 		23 0 2 3.8E-02 0 0
CUI: C0242526
Disease: Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, 45,X 		23 0 2 3.8E-02 0 0
CUI: C1392786
Disease: Cognitive changes
Cognitive changes 		50 0 3 3.8E-02 0 0
CUI: C3544321
Disease: Treatment-resistant schizophrenia
Treatment-resistant schizophrenia 		23 0 2 3.8E-02 0 0
CUI: C0022118
Disease: Transient ischemia
Transient ischemia 		25 0 2 3.7E-02 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		165 0 7 3.7E-02 0 0