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: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 3.1E-04 0 0
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality 		18 0 1 3.1E-04 0 0
CUI: C2712334
Disease: Actual Aspiration
Actual Aspiration 		18 0 1 3.1E-04 0 0
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		17 0 1 3.1E-04 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure 		17 0 1 3.1E-04 0 0
CUI: C3671887
Disease: Hypernatriuria
Hypernatriuria 		17 0 1 3.1E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 3.1E-04 0 0
CUI: C1609528
Disease: Restrictive deficit on pulmonary function testing
Restrictive deficit on pulmonary function testing 		16 0 1 3.1E-04 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 1 3.1E-04 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 1 3.1E-04 0 0
CUI: C3279725
Disease: Hip flexor weakness
Hip flexor weakness 		16 0 1 3.1E-04 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 1 3.1E-04 0 0
CUI: C4285716
Disease: Melatonin deficiency
Melatonin deficiency 		16 0 1 3.1E-04 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 1 3.1E-04 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 23 1 3.1E-04 1 4.8E-03
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis 		15 0 1 3.1E-04 0 0
CUI: C0025587
Disease: Metatarsalgia
Metatarsalgia 		15 0 1 3.1E-04 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 1 3.1E-04 0 0
CUI: C1856691
Disease: Impaired proprioception
Impaired proprioception 		15 0 1 3.1E-04 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 1 3.1E-04 0 0
CUI: C2749688
Disease: Abnormal isoelectric focusing of serum transferrin
Abnormal isoelectric focusing of serum transferrin 		15 0 1 3.1E-04 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 1 3.1E-04 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 1 3.1E-04 0 0
CUI: C4025615
Disease: Decreased size of nerve terminals
Decreased size of nerve terminals 		15 0 1 3.1E-04 0 0
CUI: C4531122
Disease: Abnormal speech prosody
Abnormal speech prosody 		15 0 1 3.1E-04 0 0