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: C1850451
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 1
CEROID LIPOFUSCINOSIS, NEURONAL, 1 		3 0 1 0.12 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		3 0 1 0.12 0 0
CUI: C3887518
Disease: Adult Myxopapillary Ependymoma
Adult Myxopapillary Ependymoma 		3 0 1 0.12 0 0
CUI: C4021781
Disease: Abnormal nervous system electrophysiology
Abnormal nervous system electrophysiology 		3 0 1 0.12 0 0
CUI: C4284040
Disease: FIGO Stage III Ovarian Cancer
FIGO Stage III Ovarian Cancer 		3 0 1 0.12 0 0
CUI: C1291230
Disease: 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3-Hydroxyacyl-CoA Dehydrogenase Deficiency 		4 0 1 0.11 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings 		4 0 1 0.11 0 0
CUI: C1850041
Disease: Facial hirsutism
Facial hirsutism 		4 2 1 0.11 1 1.5E-02
CUI: C2609176
Disease: Kounis Syndrome
Kounis Syndrome 		4 0 1 0.11 0 0
CUI: C0269972
Disease: Postpartum cardiomyopathy
Postpartum cardiomyopathy 		5 0 1 1.0E-01 0 0
CUI: C1836851
Disease: Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material 		5 0 1 1.0E-01 0 0
CUI: C1864923
Disease: Northern epilepsy syndrome
Northern epilepsy syndrome 		5 0 1 1.0E-01 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		51 74 5 9.6E-02 17 0.14
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 2 9.1E-02 0 0
CUI: C1850442
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 5
CEROID LIPOFUSCINOSIS, NEURONAL, 5 		6 0 1 9.1E-02 0 0
CUI: C3273225
Disease: Hereditary Neurodegenerative Disorder
Hereditary Neurodegenerative Disorder 		6 0 1 9.1E-02 0 0
CUI: C4015286
Disease: MACULAR DEGENERATION, EARLY-ONSET
MACULAR DEGENERATION, EARLY-ONSET 		6 0 1 9.1E-02 0 0
CUI: C0270913
Disease: Charcot-Marie-Tooth disease, Type 1C
Charcot-Marie-Tooth disease, Type 1C 		7 0 1 8.3E-02 0 0
CUI: C0281328
Disease: Adult Subependymoma
Adult Subependymoma 		7 0 1 8.3E-02 0 0
CUI: C0423083
Disease: Hypermetric saccades
Hypermetric saccades 		7 0 1 8.3E-02 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 2 8.0E-02 0 0
CUI: C0238051
Disease: Cerebral Angiitis
Cerebral Angiitis 		8 0 1 7.7E-02 0 0
CUI: C0268281
Disease: Infantile neuronal ceroid lipofuscinosis
Infantile neuronal ceroid lipofuscinosis 		22 0 2 7.7E-02 0 0
CUI: C0393561
Disease: Subcortical Vascular Dementia
Subcortical Vascular Dementia 		8 0 1 7.7E-02 0 0
CUI: C1836855
Disease: Vacuolated lymphocytes
Vacuolated lymphocytes 		8 0 1 7.7E-02 0 0