Source: CLINVAR ×
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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		237 0 1 4.1E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia 		11 0 1 6.2E-02 0 0
CUI: C0003578
Disease: Apnea
Apnea 		7 0 1 8.3E-02 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia 		12 0 1 5.9E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		15 0 1 5.0E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 1.7E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 1 2.0E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		15 0 1 5.0E-02 0 0
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		6 0 1 9.1E-02 0 0
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		29 0 1 2.9E-02 0 0
CUI: C0013595
Disease: Eczema
Eczema 		15 0 1 5.0E-02 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 1 7.7E-02 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 0 1 2.9E-02 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		7 0 1 8.3E-02 0 0
CUI: C0020578
Disease: Hyperventilation
Hyperventilation 		2 0 1 0.14 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		12 0 1 5.9E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		28 0 1 3.0E-02 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		162 0 1 6.0E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		336 0 2 5.9E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		19 0 1 4.2E-02 0 0
CUI: C0029453
Disease: Osteopenia
Osteopenia 		23 0 1 3.6E-02 0 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		6 0 1 9.1E-02 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		63 0 1 1.5E-02 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		43 0 1 2.1E-02 0 0
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities 		6 0 1 9.1E-02 0 0