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: C4022919
Disease: Appendicular hypotonia
Appendicular hypotonia 		7 8 2 0.18 1 7.7E-02
CUI: C0007642
Disease: Cellulitis
Cellulitis 		1 1 1 0.17 1 0.17
CUI: C0025222
Disease: Melena
Melena 		1 1 1 0.17 1 0.17
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		1 22 1 0.17 1 3.7E-02
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial 		1 0 1 0.17 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.17 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		1 0 1 0.17 0 0
CUI: C0332601
Disease: Cushingoid facies
Cushingoid facies 		1 1 1 0.17 1 0.17
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 1 1 0.17 1 0.17
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 0.17 0 0
CUI: C1142132
Disease: Carnitine deficiency
Carnitine deficiency 		1 0 1 0.17 0 0
CUI: C1608410
Disease: Head titubation
Head titubation 		1 0 1 0.17 0 0
CUI: C1735903
Disease: Chronic acidosis
Chronic acidosis 		1 1 1 0.17 1 0.17
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		1 0 1 0.17 0 0
CUI: C1839164
Disease: Thrombocytopenia, X-Linked, Intermittent
Thrombocytopenia, X-Linked, Intermittent 		1 0 1 0.17 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.17 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 0.17 0 0
CUI: C1846058
Disease: Lubs X-linked mental retardation syndrome
Lubs X-linked mental retardation syndrome 		1 0 1 0.17 0 0
CUI: C1848395
Disease: Large for gestational age
Large for gestational age 		8 10 2 0.17 1 6.7E-02
CUI: C1851808
Disease: Premature delivery because of cervical insufficiency or membrane fragility
Premature delivery because of cervical insufficiency or membrane fragility 		1 1 1 0.17 1 0.17
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail 		1 1 1 0.17 1 0.17
CUI: C1866180
Disease: Horizontal pendular nystagmus
Horizontal pendular nystagmus 		1 0 1 0.17 0 0
CUI: C1866284
Disease: Motor deterioration
Motor deterioration 		1 0 1 0.17 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 0.17 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 42 1 0.17 1 2.1E-02