Source: ALL
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 3.5E-04
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 3.5E-04
CUI: C0037826
Disease: Speech Perception
Speech Perception 		0 1 0 0 1 3.5E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 3.5E-04
CUI: C0233681
Disease: Grandiose delusions
Grandiose delusions 		0 1 0 0 1 3.5E-04
CUI: C0233720
Disease: Poverty of speech
Poverty of speech 		0 1 0 0 1 3.5E-04
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia 		0 2 0 0 1 3.5E-04
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 3.5E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.5E-04
CUI: C0476482
Disease: Restlessness and agitation
Restlessness and agitation 		0 1 0 0 1 3.5E-04
CUI: C1720994
Disease: Eye Movement Measurements
Eye Movement Measurements 		0 4 0 0 3 1.0E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 3.5E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.4E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.5E-04
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.5E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.5E-04
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 1 3.4E-04 0 0
CUI: C4025249
Disease: Abnormality of the intervertebral disk
Abnormality of the intervertebral disk 		30 0 1 3.4E-04 0 0
CUI: C0426799
Disease: Congenital hypoplasia of clavicle
Congenital hypoplasia of clavicle 		28 0 1 3.4E-04 0 0
CUI: C0426807
Disease: Short clavicle
Short clavicle 		26 0 1 3.5E-04 0 0
CUI: C1843392
Disease: Death in childhood
Death in childhood 		25 0 1 3.5E-04 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 1 3.5E-04 0 0
CUI: C3278811
Disease: Thumb aplasia
Thumb aplasia 		22 0 1 3.5E-04 0 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		21 0 1 3.5E-04 0 0
CUI: C0241391
Disease: Thumb absent
Thumb absent 		21 0 1 3.5E-04 0 0