Source: INFERRED ×
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: C0020039
Disease: Hostility
Hostility 		1 0 1 0.14 0 0
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial 		1 0 1 0.14 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.14 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		1 0 1 0.14 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 0.14 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.14 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.14 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 8 1 0.14 1 7.0E-03
CUI: C1846058
Disease: Lubs X-linked mental retardation syndrome
Lubs X-linked mental retardation syndrome 		1 8 1 0.14 2 1.4E-02
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 23 1 0.14 4 2.6E-02
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 42 1 0.14 5 2.9E-02
CUI: C2675473
Disease: Mental Retardation, Autosomal Dominant 5
Mental Retardation, Autosomal Dominant 5 		1 64 1 0.14 1 5.1E-03
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 2 1 0.14 1 7.4E-03
CUI: C3809650
Disease: BAINBRIDGE-ROPERS SYNDROME
BAINBRIDGE-ROPERS SYNDROME 		1 17 1 0.14 1 6.6E-03
CUI: C4022447
Disease: Abnormality of the tympanic membrane
Abnormality of the tympanic membrane 		1 0 1 0.14 0 0
CUI: C4022860
Disease: Maternal anticardiolipin antibody positive
Maternal anticardiolipin antibody positive 		1 0 1 0.14 0 0
CUI: C4025796
Disease: Abnormality of the fingertips
Abnormality of the fingertips 		1 1 1 0.14 1 7.4E-03
CUI: C4073241
Disease: Abnormality of nasopharyngeal adenoids
Abnormality of nasopharyngeal adenoids 		1 0 1 0.14 0 0
CUI: C4085238
Disease: MYOCLONIC-ATONIC EPILEPSY
MYOCLONIC-ATONIC EPILEPSY 		1 16 1 0.14 1 6.7E-03
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy 		2 0 1 0.12 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		2 15 1 0.12 1 6.7E-03
CUI: C1864361
Disease: Lower thoracic kyphosis
Lower thoracic kyphosis 		2 0 1 0.12 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical 		2 42 1 0.12 1 5.7E-03
CUI: C4021099
Disease: Orthostatic tachycardia
Orthostatic tachycardia 		2 0 1 0.12 0 0
CUI: C4022750
Disease: Thin fingernail
Thin fingernail 		2 0 1 0.12 0 0