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: C0038131
Disease: Stammering
Stammering 		1 0 1 0.50 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 0.50 0 0
CUI: C0477972
Disease: Other specified congenital malformations of brain
Other specified congenital malformations of brain 		1 0 1 0.50 0 0
CUI: C0751527
Disease: Stuttering, Adult
Stuttering, Adult 		1 0 1 0.50 0 0
CUI: C2750246
Disease: Pitt-Hopkins-Like Syndrome 1
Pitt-Hopkins-Like Syndrome 1 		1 0 1 0.50 0 0
CUI: C2910100
Disease: Arnold-Chiari syndrome, type IV
Arnold-Chiari syndrome, type IV 		1 0 1 0.50 0 0
CUI: C3539123
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 11
CEROID LIPOFUSCINOSIS, NEURONAL, 11 		1 0 1 0.50 0 0
CUI: C4303804
Disease: Deficiency of cathepsin D
Deficiency of cathepsin D 		1 0 1 0.50 0 0
CUI: C4552043
Disease: Cortical dysplasia with focal epilepsy syndrome
Cortical dysplasia with focal epilepsy syndrome 		1 0 1 0.50 0 0
CUI: C4751168
Disease: Pitt Hopkins-like syndrome
Pitt Hopkins-like syndrome 		1 0 1 0.50 0 0
CUI: C0562457
Disease: Manic behavior
Manic behavior 		2 0 1 0.33 0 0
CUI: C3489627
Disease: Stuttering, Familial Persistent 1
Stuttering, Familial Persistent 1 		2 0 1 0.33 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 0.25 0 0
CUI: C0751528
Disease: Stuttering, Childhood
Stuttering, Childhood 		3 0 1 0.25 0 0
CUI: C1850792
Disease: Congenital myasthenic syndrome ib
Congenital myasthenic syndrome ib 		3 0 1 0.25 0 0
CUI: C2930824
Disease: Autoimmune limbic encephalitis
Autoimmune limbic encephalitis 		3 0 1 0.25 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia 		3 0 1 0.25 0 0
CUI: C0268279
Disease: Lipofuscinosis
Lipofuscinosis 		4 0 1 0.20 0 0
CUI: C0349391
Disease: Apraxia, Verbal
Apraxia, Verbal 		4 0 1 0.20 0 0
CUI: C0751919
Disease: Acquired Neuromyotonia
Acquired Neuromyotonia 		4 0 1 0.20 0 0
CUI: C1857280
Disease: Infra-orbital crease
Infra-orbital crease 		4 0 1 0.20 0 0
CUI: C3854373
Disease: Morvan syndrome
Morvan syndrome 		4 0 1 0.20 0 0
CUI: C4274665
Disease: Logopenic progressive aphasia
Logopenic progressive aphasia 		4 0 1 0.20 0 0
CUI: C0239154
Disease: High pitched cry
High pitched cry 		5 0 1 0.17 0 0
CUI: C0478658
Disease: Disorder of psychological development
Disorder of psychological development 		5 0 1 0.17 0 0