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: C0268563
Disease: Sarcosinemia
Sarcosinemia
4 0 4 0.20 0 0
CUI: C0032268
Disease: Pneumocephalus
Pneumocephalus
6 0 4 0.18 0 0
CUI: C0007279
Disease: Carotid Body Paraganglioma
Carotid Body Paraganglioma
7 0 4 0.17 0 0
CUI: C0236053
Disease: Mucosal ulcer
Mucosal ulcer
15 0 5 0.17 0 0
Succinate-coenzyme Q reductase deficiency
8 0 4 0.17 0 0
CUI: C1533592
Disease: Malignant Paraganglionic Neoplasm
Malignant Paraganglionic Neoplasm
8 0 4 0.17 0 0
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency
8 0 4 0.17 0 0
CUI: C3697716
Disease: Acute flaccid paralysis
Acute flaccid paralysis
10 0 4 0.15 0 0
CUI: C0270726
Disease: Alexander Disease
Alexander Disease
27 0 6 0.15 0 0
CUI: C0030422
Disease: Extra-Adrenal Paraganglioma
Extra-Adrenal Paraganglioma
12 0 4 0.14 0 0
CUI: C0920193
Disease: Photodermatosis
Photodermatosis
4 0 3 0.14 0 0
Cervical Glandular Intraepithelial Neoplasia
4 0 3 0.14 0 0
CUI: C0332983
Disease: Malassez' epithelial rests
Malassez' epithelial rests
6 0 3 0.13 0 0
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
6 0 3 0.13 0 0
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
6 0 3 0.13 0 0
CUI: C1333993
Disease: hereditary paraganglioma
hereditary paraganglioma
15 0 4 0.13 0 0
CUI: C0858009
Disease: Mumps virus infection
Mumps virus infection
8 0 3 0.12 0 0
Distal Hereditary Motor Neuropathy, Type II
8 0 3 0.12 0 0
CUI: C0278511
Disease: Osteosarcoma localised
Osteosarcoma localised
9 0 3 0.12 0 0
CUI: C1333944
Disease: Paraganglioma of head and neck
Paraganglioma of head and neck
19 0 4 0.11 0 0
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs
19 0 4 0.11 0 0
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension
21 0 4 0.11 0 0
CUI: C3544266
Disease: Hepatobiliary cancer
Hepatobiliary cancer
11 0 3 0.11 0 0
CUI: C0745133
Disease: Isolated systolic hypertension
Isolated systolic hypertension
22 0 4 0.11 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy
12 0 3 0.10 0 0