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: C1708957
Disease: Mediastinal Paraganglioma
Mediastinal Paraganglioma
5 0 5 0.83 0 0
CUI: C3203503
Disease: Mixed delirium
Mixed delirium
5 0 5 0.83 0 0
cutaneous squamous cell carcinoma of the head and neck
6 0 5 0.71 0 0
CUI: C0678255
Disease: polydrug use
polydrug use
7 0 5 0.62 0 0
CUI: C3203501
Disease: Hypoactive delirium
Hypoactive delirium
7 0 5 0.62 0 0
Locally Metastatic Malignant Neoplasm
8 0 5 0.56 0 0
CUI: C1855263
Disease: Disorganized thinking
Disorganized thinking
8 0 5 0.56 0 0
CUI: C1837610
Disease: ICHTHYOSIS PREMATURITY SYNDROME
ICHTHYOSIS PREMATURITY SYNDROME
9 0 5 0.50 0 0
Adult onset autosomal dominant leukodystrophy
9 0 5 0.50 0 0
CUI: C3826614
Disease: Cardiac arrest in children
Cardiac arrest in children
4 0 3 0.43 0 0
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III
5 0 3 0.38 0 0
CUI: C0339084
Disease: Floppy lid syndrome
Floppy lid syndrome
6 0 3 0.33 0 0
CUI: C0149887
Disease: Slipped Capital Femoral Epiphyses
Slipped Capital Femoral Epiphyses
15 0 5 0.31 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder)
16 0 5 0.29 0 0
CUI: C0233705
Disease: Cancerophobia
Cancerophobia
17 0 5 0.28 0 0
CUI: C1504431
Disease: Idiopathic pneumonia syndrome
Idiopathic pneumonia syndrome
18 0 5 0.26 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome
20 0 5 0.24 0 0
NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME
13 0 3 0.19 0 0
CUI: C0031391
Disease: Phencyclidine Abuse
Phencyclidine Abuse
7 0 2 0.18 0 0
CUI: C0236742
Disease: Phencyclidine-Related Disorders
Phencyclidine-Related Disorders
7 0 2 0.18 0 0
CUI: C0340828
Disease: Capillary-venous malformation
Capillary-venous malformation
1 0 1 0.17 0 0
CUI: C1861790
Disease: Hepatic vascular malformations
Hepatic vascular malformations
1 0 1 0.17 0 0
CUI: C1861791
Disease: Retinal vascular malformation
Retinal vascular malformation
1 0 1 0.17 0 0
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4
1 0 1 0.17 0 0
CUI: C4015671
Disease: LONG QT SYNDROME 14
LONG QT SYNDROME 14
1 0 1 0.17 0 0