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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 9.0E-04
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 9.0E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 2 1.8E-03
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 9.0E-04
CUI: C0373601
Disease: Dihydrotestosterone Assay
Dihydrotestosterone Assay 		0 2 0 0 1 9.0E-04
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias 		0 19 0 0 1 8.9E-04
CUI: C1841621
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1 		0 20 0 0 1 8.8E-04
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0 14 0 0 1 8.9E-04
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 9.0E-04
CUI: C3151417
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6 		0 1 0 0 1 9.0E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 9.0E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 9.0E-04
CUI: C4016190
Disease: DELTA-PLUS-THALASSEMIA
DELTA-PLUS-THALASSEMIA 		0 1 0 0 1 9.0E-04
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 9.0E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 9.0E-04
CUI: C4693797
Disease: METHEMOGLOBINEMIA, BETA TYPE
METHEMOGLOBINEMIA, BETA TYPE 		0 13 0 0 1 8.9E-04
CUI: C4693822
Disease: ERYTHROCYTOSIS, FAMILIAL, 6
ERYTHROCYTOSIS, FAMILIAL, 6 		0 39 0 0 1 8.7E-04
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 3.5E-04 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 3.5E-04 0 0
CUI: C1839888
Disease: Decreased activity of the pyruvate dehydrogenase complex
Decreased activity of the pyruvate dehydrogenase complex 		35 0 1 3.5E-04 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy 		24 0 1 3.5E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 3.5E-04 0 0
CUI: C0343073
Disease: Wooly hair
Wooly hair 		19 0 1 3.5E-04 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 1 3.5E-04 0 0
CUI: C0023067
Disease: Laryngitis
Laryngitis 		17 0 1 3.5E-04 0 0