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: C0085997
Disease: Child Development Disorders, Specific
Child Development Disorders, Specific 		30 0 29 0.97 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		355 0 29 8.2E-02 0 0
CUI: C3696898
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 		17 0 3 7.0E-02 0 0
CUI: C0751460
Disease: Flaccid Quadriplegia
Flaccid Quadriplegia 		2 0 2 6.9E-02 0 0
CUI: C0751461
Disease: Paralysis, Spinal, Quadriplegic
Paralysis, Spinal, Quadriplegic 		2 0 2 6.9E-02 0 0
CUI: C0265482
Disease: Ring Chromosome 20 Syndrome
Ring Chromosome 20 Syndrome 		3 0 2 6.7E-02 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		35 0 4 6.7E-02 0 0
CUI: C0393671
Disease: Frontal Epilepsy, Benign, Childhood
Frontal Epilepsy, Benign, Childhood 		4 0 2 6.5E-02 0 0
CUI: C0393683
Disease: Epilepsy, Supplementary Motor
Epilepsy, Supplementary Motor 		4 0 2 6.5E-02 0 0
CUI: C0393684
Disease: Epilepsy, Cingulate
Epilepsy, Cingulate 		4 0 2 6.5E-02 0 0
CUI: C0393688
Disease: Epilepsy, Opercular
Epilepsy, Opercular 		4 0 2 6.5E-02 0 0
CUI: C0751642
Disease: Epilepsy, Anterior Fronto-Polar
Epilepsy, Anterior Fronto-Polar 		4 0 2 6.5E-02 0 0
CUI: C0751643
Disease: Epilepsy, Orbito-Frontal
Epilepsy, Orbito-Frontal 		4 0 2 6.5E-02 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		73 0 6 6.2E-02 0 0
CUI: C0023944
Disease: Locked-In Syndrome
Locked-In Syndrome 		5 0 2 6.2E-02 0 0
CUI: C1321905
Disease: Minimal Brain Dysfunction
Minimal Brain Dysfunction 		22 0 3 6.2E-02 0 0
CUI: C0034372
Disease: Quadriplegia
Quadriplegia 		57 0 5 6.2E-02 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		40 0 4 6.2E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		40 0 4 6.2E-02 0 0
CUI: C0006325
Disease: Bruxism
Bruxism 		24 0 3 6.0E-02 0 0
CUI: C0349578
Disease: Complex Endometrial Hyperplasia
Complex Endometrial Hyperplasia 		7 0 2 5.9E-02 0 0
CUI: C0751349
Disease: Myoclonus, Eyelid
Myoclonus, Eyelid 		7 0 2 5.9E-02 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 2 5.9E-02 0 0
CUI: C0026613
Disease: Motor Skills Disorders
Motor Skills Disorders 		8 0 2 5.7E-02 0 0
CUI: C0022333
Disease: Jacksonian Seizure
Jacksonian Seizure 		102 0 7 5.6E-02 0 0