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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 9.2E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 9.2E-04
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 9.2E-04
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance
0 1 0 0 1 9.2E-04
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases
0 1 0 0 1 9.2E-04
CUI: C1456582
Disease: Vision Impairment and Blindness
Vision Impairment and Blindness
0 1 0 0 1 9.2E-04
ALDOSTERONE TO RENIN RATIO, INCREASED
0 1 0 0 1 9.2E-04
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder)
0 1 0 0 1 9.2E-04
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10 (finding)
0 2 0 0 1 9.2E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 3 2.8E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 9.2E-04
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism
0 2 0 0 1 9.2E-04
CUI: C4016190
Disease: DELTA-PLUS-THALASSEMIA
DELTA-PLUS-THALASSEMIA
0 1 0 0 1 9.2E-04
HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH EXACERBATION IN PREGNANCY
0 1 0 0 1 9.2E-04
Frequent episodic tension-type headache
0 1 0 0 1 9.2E-04
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination
32 0 1 4.2E-04 0 0
CUI: C1844527
Disease: Clitoral hypoplasia
Clitoral hypoplasia
30 0 1 4.3E-04 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
24 0 1 4.3E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes
23 0 1 4.3E-04 0 0
CUI: C0919909
Disease: Tonic clonic movements
Tonic clonic movements
22 0 1 4.3E-04 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia
21 0 1 4.3E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin
21 0 1 4.3E-04 0 0
CUI: C1879312
Disease: Agyria
Agyria
20 0 1 4.3E-04 0 0
Juvenile amyotrophic lateral sclerosis
20 0 1 4.3E-04 0 0
CUI: C0334013
Disease: Phrynoderma
Phrynoderma
19 0 1 4.3E-04 0 0