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: C0752289
Disease: Environmental Sleep Disorder
Environmental Sleep Disorder 		1 0 1 0.14 0 0
CUI: C0752291
Disease: Limit-Setting Sleep Disorder
Limit-Setting Sleep Disorder 		1 0 1 0.14 0 0
CUI: C0752292
Disease: Nocturnal Eating-Drinking Syndrome
Nocturnal Eating-Drinking Syndrome 		1 0 1 0.14 0 0
CUI: C0752293
Disease: Sleep Disorders, Extrinsic
Sleep Disorders, Extrinsic 		1 0 1 0.14 0 0
CUI: C0854492
Disease: Tertiary hypothyroidism
Tertiary hypothyroidism 		1 0 1 0.14 0 0
CUI: C1275836
Disease: D - transposition of the great vessels
D - transposition of the great vessels 		1 0 1 0.14 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 0.14 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 0.14 0 0
CUI: C1457871
Disease: Sarcoid arthritis
Sarcoid arthritis 		1 0 1 0.14 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.14 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 0.14 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 0.14 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 0.14 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		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 0 1 0.14 0 0
CUI: C1847886
Disease: Anomalous branches of internal carotid artery
Anomalous branches of internal carotid artery 		1 1 1 0.14 1 0.33
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 0.14 0 0
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 0.14 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 43 1 0.14 1 2.2E-02
CUI: C2129647
Disease: menstrual symptoms
menstrual symptoms 		1 0 1 0.14 0 0
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 0 1 0.14 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.14 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 0.14 0 0
CUI: C3150700
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 20
MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 		1 0 1 0.14 0 0