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: C3809672
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37 		2 0 1 0.20 0 0
CUI: C0010598
Disease: Cyclothymic Disorder
Cyclothymic Disorder 		4 0 1 0.14 0 0
CUI: C1334970
Disease: Medulloblastoma with extensive nodularity
Medulloblastoma with extensive nodularity 		4 0 1 0.14 0 0
CUI: C0814154
Disease: Alcohol Related Neurodevelopmental Disorder
Alcohol Related Neurodevelopmental Disorder 		5 0 1 0.12 0 0
CUI: C3661483
Disease: Partial Fetal Alcohol Syndrome
Partial Fetal Alcohol Syndrome 		5 0 1 0.12 0 0
CUI: C0410204
Disease: Myopathy, Centronuclear, Autosomal Recessive
Myopathy, Centronuclear, Autosomal Recessive 		6 0 1 0.11 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 1 1.0E-01 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 0 1 1.0E-01 0 0
CUI: C0231531
Disease: Muscle fibrillation
Muscle fibrillation 		8 0 1 9.1E-02 0 0
CUI: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID 		8 0 1 9.1E-02 0 0
CUI: C1853934
Disease: Deposits immunoreactive to beta-amyloid protein
Deposits immunoreactive to beta-amyloid protein 		8 0 1 9.1E-02 0 0
CUI: C3146244
Disease: Alcohol Related Birth Defect
Alcohol Related Birth Defect 		8 0 1 9.1E-02 0 0
CUI: C4025785
Disease: Abnormality of the foot musculature
Abnormality of the foot musculature 		8 0 1 9.1E-02 0 0
CUI: C0410226
Disease: Congenital Myotonic Dystrophy
Congenital Myotonic Dystrophy 		9 0 1 8.3E-02 0 0
CUI: C3839736
Disease: Sensitization (disorder)
Sensitization (disorder) 		9 0 1 8.3E-02 0 0
CUI: C1836599
Disease: Macrocephaly at birth
Macrocephaly at birth 		12 0 1 6.7E-02 0 0
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		12 0 1 6.7E-02 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 1 6.2E-02 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 1 6.2E-02 0 0
CUI: C0027858
Disease: Neuroma
Neuroma 		15 0 1 5.6E-02 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 1 5.3E-02 0 0
CUI: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 1 5.3E-02 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		18 0 1 4.8E-02 0 0
CUI: C1954751
Disease: Microdeletion syndromes
Microdeletion syndromes 		18 0 1 4.8E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior 		19 0 1 4.5E-02 0 0