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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		0 4 0 0 1 2.6E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.9E-02
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland 		0 4 0 0 1 2.6E-02
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 2.9E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 2 5.7E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 5.7E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 2.8E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 2.8E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.9E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 2.7E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 591 1 2.0E-03 1 1.6E-03
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.2E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.2E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 2.2E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.4E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 2.4E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.4E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.4E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 1 2.4E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.5E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.5E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 0 1 2.5E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.5E-03 0 0