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: C3280282
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT 		1 0 1 0.14 0 0
CUI: C4310643
Disease: NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE 		1 0 1 0.14 0 0
CUI: C4539843
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55 		1 0 1 0.14 0 0
CUI: C4693325
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE 		1 0 1 0.14 0 0
CUI: C4693964
Disease: NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE 		1 0 1 0.14 0 0
CUI: C4748427
Disease: SQUALENE SYNTHASE DEFICIENCY
SQUALENE SYNTHASE DEFICIENCY 		1 0 1 0.14 0 0
CUI: C0406756
Disease: Keratolytic winter erythema
Keratolytic winter erythema 		2 0 1 0.12 0 0
CUI: C1846135
Disease: Autistic features
Autistic features 		3 0 1 0.11 0 0
CUI: C1959626
Disease: Mevalonic Aciduria
Mevalonic Aciduria 		3 0 1 0.11 0 0
CUI: C2931048
Disease: HEM dysplasia
HEM dysplasia 		3 0 1 0.11 0 0
CUI: C4707565
Disease: Bilateral polymicrogyria
Bilateral polymicrogyria 		3 0 1 0.11 0 0
CUI: C0085620
Disease: Flaccid paralysis
Flaccid paralysis 		4 0 1 1.0E-01 0 0
CUI: C1704268
Disease: Delusion of persecution
Delusion of persecution 		4 0 1 1.0E-01 0 0
CUI: C1864652
Disease: Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate 		4 0 1 1.0E-01 0 0
CUI: C4022387
Disease: Recurrent hand flapping
Recurrent hand flapping 		4 0 1 1.0E-01 0 0
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 1 9.1E-02 0 0
CUI: C0265267
Disease: Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 		6 0 1 8.3E-02 0 0
CUI: C0031391
Disease: Phencyclidine Abuse
Phencyclidine Abuse 		7 0 1 7.7E-02 0 0
CUI: C0236742
Disease: Phencyclidine-Related Disorders
Phencyclidine-Related Disorders 		7 0 1 7.7E-02 0 0
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis 		9 0 1 6.7E-02 0 0
CUI: C0268146
Disease: Glucose-6-phosphate transport defect
Glucose-6-phosphate transport defect 		9 0 1 6.7E-02 0 0
CUI: C0282102
Disease: Chondrodysplasia punctata, X-linked dominant type
Chondrodysplasia punctata, X-linked dominant type 		9 0 1 6.7E-02 0 0
CUI: C4225275
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 40
MENTAL RETARDATION, AUTOSOMAL DOMINANT 40 		9 0 1 6.7E-02 0 0
CUI: C0018614
Disease: Hashish Abuse
Hashish Abuse 		10 0 1 6.2E-02 0 0
CUI: C0236735
Disease: Cannabis-Related Disorder
Cannabis-Related Disorder 		10 0 1 6.2E-02 0 0