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: C0422895
Disease: Primitive reflex
Primitive reflex 		14 0 14 1.00 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior 		14 0 4 0.17 0 0
CUI: C1855353
Disease: Fixed facial expression
Fixed facial expression 		2 0 2 0.14 0 0
CUI: C3714237
Disease: Trifunctional Protein Deficiency, Type 2
Trifunctional Protein Deficiency, Type 2 		2 0 2 0.14 0 0
CUI: C0474420
Disease: Inappropriate sexual behavior
Inappropriate sexual behavior 		3 0 2 0.13 0 0
CUI: C1860449
Disease: Equinus calcaneus
Equinus calcaneus 		3 0 2 0.13 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia 		3 0 2 0.13 0 0
CUI: C1849686
Disease: Diffuse hepatic steatosis
Diffuse hepatic steatosis 		4 0 2 0.12 0 0
CUI: C4021584
Disease: Frontotemporal cerebral atrophy
Frontotemporal cerebral atrophy 		14 0 3 0.12 0 0
CUI: C1858116
Disease: Caudate atrophy
Caudate atrophy 		6 0 2 0.11 0 0
CUI: C4021582
Disease: Distal peripheral sensory neuropathy
Distal peripheral sensory neuropathy 		6 0 2 0.11 0 0
CUI: C4551566
Disease: Equinovarus deformity of foot
Equinovarus deformity of foot 		6 0 2 0.11 0 0
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter 		7 0 2 0.11 0 0
CUI: C1838579
Disease: Pseudobulbar signs
Pseudobulbar signs 		7 0 2 0.11 0 0
CUI: C1858680
Disease: Familial encephalopathy with neuroserpin inclusion bodies
Familial encephalopathy with neuroserpin inclusion bodies 		7 0 2 0.11 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 3 0.10 0 0
CUI: C0003113
Disease: Anomia
Anomia 		8 0 2 1.0E-01 0 0
CUI: C0234502
Disease: Visual Agnosia
Visual Agnosia 		8 0 2 1.0E-01 0 0
CUI: C0266781
Disease: Abnormal amniotic fluid
Abnormal amniotic fluid 		8 0 2 1.0E-01 0 0
CUI: C0338630
Disease: Senile Paranoid Dementia
Senile Paranoid Dementia 		8 0 2 1.0E-01 0 0
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex 		8 0 2 1.0E-01 0 0
CUI: C3711645
Disease: Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 		8 0 2 1.0E-01 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit 		8 0 2 1.0E-01 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 3 9.7E-02 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 2 9.5E-02 0 0