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 3.6E-02 0 0
CUI: C0040124
Disease: Thyroglossal Cyst
Thyroglossal Cyst 		1 0 1 3.6E-02 0 0
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial 		1 0 1 3.6E-02 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 3.6E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 3.6E-02 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		1 0 1 3.6E-02 0 0
CUI: C0349450
Disease: Soiling
Soiling 		1 0 1 3.6E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 3.6E-02 0 0
CUI: C0585216
Disease: Alpha-Thalassemia Myelodysplasia Syndrome
Alpha-Thalassemia Myelodysplasia Syndrome 		1 0 1 3.6E-02 0 0
CUI: C0596028
Disease: Overjet, Dental
Overjet, Dental 		1 0 1 3.6E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.6E-02 0 0
CUI: C0748199
Disease: Recurrent pyelonephritis
Recurrent pyelonephritis 		1 0 1 3.6E-02 0 0
CUI: C0795889
Disease: Allan-Herndon-Dudley syndrome (AHDS)
Allan-Herndon-Dudley syndrome (AHDS) 		1 25 1 3.6E-02 1 1.7E-02
CUI: C0796003
Disease: Juberg-Marsidi syndrome
Juberg-Marsidi syndrome 		1 6 1 3.6E-02 1 2.4E-02
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		1 0 1 3.6E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 3.6E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 3.6E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 3.6E-02 0 0
CUI: C1837341
Disease: Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 1 		1 0 1 3.6E-02 0 0
CUI: C1842534
Disease: DYSTONIA 18 (disorder)
DYSTONIA 18 (disorder) 		1 0 1 3.6E-02 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 3.6E-02 0 0
CUI: C1845055
Disease: ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED 		1 21 1 3.6E-02 1 1.8E-02
CUI: C1845243
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE 		1 0 1 3.6E-02 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 3.6E-02 0 0
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		1 0 1 3.6E-02 0 0