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: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses
51 74 20 0.24 12 8.9E-02
Late-Infantile Neuronal Ceroid Lipfuscinosis
19 0 13 0.22 0 0
Adult Neuronal Ceroid Lipofuscinosis
16 0 12 0.21 0 0
Increased neuronal autofluorescent lipopigment
8 0 7 0.13 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases
130 0 16 9.6E-02 0 0
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
6 0 5 9.4E-02 0 0
Infantile neuronal ceroid lipofuscinosis
22 0 6 8.8E-02 0 0
Ceroid Lipofuscinosis, Neuronal, Parry Type
5 0 4 7.5E-02 0 0
CUI: C1838570
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 8
CEROID LIPOFUSCINOSIS, NEURONAL, 8
5 0 4 7.5E-02 0 0
CUI: C1864923
Disease: Northern epilepsy syndrome
Northern epilepsy syndrome
5 0 4 7.5E-02 0 0
CUI: C1850442
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 5
CEROID LIPOFUSCINOSIS, NEURONAL, 5
6 0 4 7.4E-02 0 0
CUI: C1876161
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 2
CEROID LIPOFUSCINOSIS, NEURONAL, 2
6 0 4 7.4E-02 0 0
CUI: C0162672
Disease: MERRF Syndrome
MERRF Syndrome
51 0 7 7.3E-02 0 0
CUI: C1866282
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 6
CEROID LIPOFUSCINOSIS, NEURONAL, 6
9 0 4 7.0E-02 0 0
CUI: C0011263
Disease: Multi-infarct dementia
Multi-infarct dementia
30 0 5 6.5E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease
92 0 8 5.9E-02 0 0
CUI: C1838571
Disease: Ceroid Lipofuscinosis, Neuronal, 7
Ceroid Lipofuscinosis, Neuronal, 7
3 0 3 5.8E-02 0 0
Abnormal nervous system electrophysiology
3 0 3 5.8E-02 0 0
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
5 0 3 5.6E-02 0 0
CUI: C0234213
Disease: Sensory denervation disorder
Sensory denervation disorder
29 0 4 5.2E-02 0 0
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1
10 0 3 5.1E-02 0 0
CUI: C0265706
Disease: Gastroschisis
Gastroschisis
31 0 4 5.1E-02 0 0
CUI: C0032027
Disease: Pityriasis Rubra Pilaris
Pityriasis Rubra Pilaris
32 0 4 5.0E-02 0 0
CUI: C1839454
Disease: PROPERDIN DEFICIENCY, X-LINKED
PROPERDIN DEFICIENCY, X-LINKED
11 0 3 5.0E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss
77 0 6 4.9E-02 0 0