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 5.1E-04
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0 6 0 0 1 5.1E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 5.1E-04
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 5.1E-04
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 5.1E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 5.1E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 1.0E-03
CUI: C0728877
Disease: Serum albumin level
Serum albumin level 		0 9 0 0 1 5.1E-04
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 5.1E-04
CUI: C1275149
Disease: Multiple skin tags
Multiple skin tags 		0 1 0 0 1 5.1E-04
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 5.1E-04
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 5.1E-04
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		0 2 0 0 1 5.1E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 5.1E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.1E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 5.1E-04
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 1.8E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		19 0 1 1.8E-04 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue 		18 0 1 1.8E-04 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 1 1.8E-04 0 0
CUI: C2230441
Disease: Triceps weakness
Triceps weakness 		18 0 1 1.8E-04 0 0
CUI: C0431384
Disease: Colpocephaly
Colpocephaly 		17 0 1 1.8E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 1.8E-04 0 0
CUI: C1846449
Disease: Irregular epiphyses
Irregular epiphyses 		15 0 1 1.8E-04 0 0
CUI: C3279397
Disease: Very long chain fatty acid accumulation
Very long chain fatty acid accumulation 		15 0 1 1.8E-04 0 0