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: C0544755
Disease: Genu varum
Genu varum 		60 0 1 1.9E-03 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 1.9E-03 0 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 0 1 1.9E-03 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 1 1.9E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.9E-03 0 0
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		57 0 1 1.9E-03 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 1 1.9E-03 0 0
CUI: C0424166
Disease: Social Anxiety
Social Anxiety 		57 0 1 1.9E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 1.9E-03 0 0
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		55 0 1 1.9E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		55 0 1 1.9E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 1.9E-03 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 0 1 1.9E-03 0 0
CUI: C0403824
Disease: Teratozoospermia
Teratozoospermia 		53 0 1 1.9E-03 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 1.9E-03 0 0
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		51 0 1 1.9E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 1.9E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 1.9E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 1.9E-03 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 1 1.9E-03 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism 		50 0 1 1.9E-03 0 0
CUI: C0162674
Disease: Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia 		50 0 1 1.9E-03 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 1 1.9E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 1.9E-03 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality 		49 0 1 1.9E-03 0 0