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: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 5.9E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 5.7E-03
CUI: C4225179
Disease: COWDEN SYNDROME 7
COWDEN SYNDROME 7 		0 3 0 0 1 5.8E-03
CUI: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 1.5E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 1.5E-04 0 0
CUI: C1839071
Disease: Spermatogenic Failure, Nonobstructive, Y-Linked
Spermatogenic Failure, Nonobstructive, Y-Linked 		16 0 1 1.5E-04 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia 		15 0 1 1.5E-04 0 0
CUI: C3279397
Disease: Very long chain fatty acid accumulation
Very long chain fatty acid accumulation 		15 0 1 1.5E-04 0 0
CUI: C1303007
Disease: Brushfield spots
Brushfield spots 		14 0 1 1.5E-04 0 0
CUI: C1836373
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K 		14 0 1 1.5E-04 0 0
CUI: C1839532
Disease: Low plasma citrulline
Low plasma citrulline 		14 0 1 1.5E-04 0 0
CUI: C4284790
Disease: Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 		14 0 1 1.5E-04 0 0
CUI: C0393519
Disease: Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Early Onset 		12 0 1 1.5E-04 0 0
CUI: C1820737
Disease: Temperature instability
Temperature instability 		12 0 1 1.5E-04 0 0
CUI: C4021795
Disease: Abnormality of Krebs cycle metabolism
Abnormality of Krebs cycle metabolism 		12 0 1 1.5E-04 0 0
CUI: C4023698
Disease: Everted upper lip vermilion
Everted upper lip vermilion 		12 0 1 1.5E-04 0 0
CUI: C4025585
Disease: Lacticaciduria
Lacticaciduria 		12 0 1 1.5E-04 0 0
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		11 0 1 1.5E-04 0 0
CUI: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 1 1.5E-04 0 0
CUI: C1859341
Disease: Olivopontocerebellar hypoplasia
Olivopontocerebellar hypoplasia 		11 0 1 1.5E-04 0 0
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section 		11 0 1 1.5E-04 0 0
CUI: C0201512
Disease: Thyroglobulin antibody measurement
Thyroglobulin antibody measurement 		10 0 1 1.5E-04 0 0
CUI: C0202159
Disease: Parathyroid hormone measurement
Parathyroid hormone measurement 		10 0 1 1.5E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency 		10 0 1 1.5E-04 0 0
CUI: C0700078
Disease: Decreased tendon reflex
Decreased tendon reflex 		10 0 1 1.5E-04 0 0