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: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		18 0 1 4.3E-04 0 0
CUI: C0201983
Disease: Dehydroepiandrosterone sulfate measurement (procedure)
Dehydroepiandrosterone sulfate measurement (procedure) 		18 0 1 4.3E-04 0 0
CUI: C0239804
Disease: White hair
White hair 		18 0 1 4.3E-04 0 0
CUI: C0266537
Disease: Congenital lamellar cataract
Congenital lamellar cataract 		18 0 1 4.3E-04 0 0
CUI: C4022792
Disease: Reduced ejection fraction
Reduced ejection fraction 		18 0 1 4.3E-04 0 0
CUI: C4023499
Disease: Generalized clonic seizures
Generalized clonic seizures 		18 0 1 4.3E-04 0 0
CUI: C4024601
Disease: Weakness of long finger extensor muscles
Weakness of long finger extensor muscles 		18 0 1 4.3E-04 0 0
CUI: C0431384
Disease: Colpocephaly
Colpocephaly 		17 0 1 4.3E-04 0 0
CUI: C1857632
Disease: Narrow palm
Narrow palm 		17 0 1 4.3E-04 0 0
CUI: C4021626
Disease: Lethal skeletal dysplasia
Lethal skeletal dysplasia 		17 0 1 4.3E-04 0 0
CUI: C0011430
Disease: Dentin Dysplasia
Dentin Dysplasia 		16 0 1 4.3E-04 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		16 0 1 4.3E-04 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 1 4.3E-04 0 0
CUI: C0302254
Disease: Juvenile cataract
Juvenile cataract 		16 0 1 4.3E-04 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 0 1 4.3E-04 0 0
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		16 0 1 4.3E-04 0 0
CUI: C1266128
Disease: Ossifying fibromyxoid tumor
Ossifying fibromyxoid tumor 		16 0 1 4.3E-04 0 0
CUI: C1318881
Disease: Vancomycin intermediate staphylococcus aureus infection
Vancomycin intermediate staphylococcus aureus infection 		16 0 1 4.3E-04 0 0
CUI: C1832119
Disease: Fibular hypoplasia
Fibular hypoplasia 		16 0 1 4.3E-04 0 0
CUI: C1839730
Disease: Prieto X-linked mental retardation syndrome
Prieto X-linked mental retardation syndrome 		16 0 1 4.3E-04 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 1 4.3E-04 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2 		16 0 1 4.3E-04 0 0
CUI: C4285716
Disease: Melatonin deficiency
Melatonin deficiency 		16 0 1 4.3E-04 0 0
CUI: C4317152
Disease: Dimple chin
Dimple chin 		16 0 1 4.3E-04 0 0
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly 		15 0 1 4.3E-04 0 0