Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Ceroid lipofuscinosis, neuronal 1, infantile
14 1 8 0.29 1 0.25
Ceroid Lipofuscinosis, Neuronal, Parry Type
5 0 4 0.17 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses
51 74 10 0.16 2 2.6E-02
Increased neuronal autofluorescent lipopigment
8 0 4 0.15 0 0
Adult Neuronal Ceroid Lipofuscinosis
16 0 5 0.15 0 0
Late-Infantile Neuronal Ceroid Lipfuscinosis
19 0 5 0.14 0 0
CUI: C1850451
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 1
CEROID LIPOFUSCINOSIS, NEURONAL, 1
3 86 3 0.14 4 4.7E-02
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
6 0 3 0.12 0 0
CUI: C0553642
Disease: Soft tissue rheumatism
Soft tissue rheumatism
9 0 3 0.11 0 0
CUI: C0271815
Disease: Postpartum Thyroiditis
Postpartum Thyroiditis
13 0 3 9.4E-02 0 0
CUI: C0231813
Disease: Meningitic respiration
Meningitic respiration
2 0 2 9.1E-02 0 0
Increased extraneuronal autofluorescent lipopigment
2 0 2 9.1E-02 0 0
Juvenile Neuronal Ceroid Lipofuscinosis
52 0 6 8.8E-02 0 0
CUI: C1288350
Disease: Subretinal membrane
Subretinal membrane
3 0 2 8.7E-02 0 0
Abnormal nervous system electrophysiology
3 0 2 8.7E-02 0 0
CUI: C1504559
Disease: Retinal gliosis
Retinal gliosis
4 0 2 8.3E-02 0 0
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
5 0 2 8.0E-02 0 0
CUI: C1876161
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 2
CEROID LIPOFUSCINOSIS, NEURONAL, 2
6 0 2 7.7E-02 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram
21 0 3 7.5E-02 0 0
CUI: C0042035
Disease: Urination Disorders
Urination Disorders
8 0 2 7.1E-02 0 0
CUI: C2674737
Disease: Abnormality of finger
Abnormality of finger
8 0 2 7.1E-02 0 0
CUI: C4024710
Disease: Cerebellar cortical atrophy
Cerebellar cortical atrophy
9 0 2 6.9E-02 0 0
CUI: C0038874
Disease: Supratentorial Neoplasms
Supratentorial Neoplasms
12 0 2 6.2E-02 0 0
CUI: C0392678
Disease: Swallowing problem
Swallowing problem
13 0 2 6.1E-02 0 0
CUI: C1836842
Disease: Psychomotor deterioration
Psychomotor deterioration
13 0 2 6.1E-02 0 0