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: C0013528
Disease: Echolalia
Echolalia 		39 0 27 0.36 0 0
CUI: C0026884
Disease: Mutism
Mutism 		47 0 26 0.31 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		86 0 28 0.23 0 0
CUI: C0032209
Disease: Platybasia
Platybasia 		18 0 11 0.16 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils 		12 0 10 0.15 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 11 0.15 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		13 0 10 0.15 0 0
CUI: C0919974
Disease: Abulia
Abulia 		9 0 9 0.14 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele 		9 0 9 0.14 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 12 0.14 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation 		26 0 11 0.14 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality 		10 0 9 0.14 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity 		10 0 9 0.14 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		12 0 9 0.14 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis 		12 0 9 0.14 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch 		13 0 9 0.13 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior 		14 0 9 0.13 0 0
CUI: C0424290
Disease: Compulsive hoarding
Compulsive hoarding 		14 0 9 0.13 0 0
CUI: C4021584
Disease: Frontotemporal cerebral atrophy
Frontotemporal cerebral atrophy 		14 0 9 0.13 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 10 0.13 0 0
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 10 0.13 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction 		16 0 9 0.13 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit 		8 0 8 0.13 0 0
CUI: C1842680
Disease: Small earlobe
Small earlobe 		17 0 9 0.13 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 12 0.13 0 0