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: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED 		8 0 1 9.1E-02 0 0
CUI: C1849485
Disease: Neuronal loss in the cerebral cortex
Neuronal loss in the cerebral cortex 		8 0 1 9.1E-02 0 0
CUI: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		21 0 2 8.7E-02 0 0
CUI: C0270763
Disease: Familial Motor Neuron Disease
Familial Motor Neuron Disease 		9 0 1 8.3E-02 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy 		9 0 1 8.3E-02 0 0
CUI: C0030442
Disease: Progressive bulbar palsy
Progressive bulbar palsy 		10 0 1 7.7E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 1 7.7E-02 0 0
CUI: C0241423
Disease: Atrophy of tongue
Atrophy of tongue 		10 0 1 7.7E-02 0 0
CUI: C0265218
Disease: Neu-Laxova syndrome
Neu-Laxova syndrome 		10 0 1 7.7E-02 0 0
CUI: C0265309
Disease: Leri-Weill dyschondrosteosis
Leri-Weill dyschondrosteosis 		10 0 1 7.7E-02 0 0
CUI: C1867773
Disease: CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 		10 0 1 7.7E-02 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 2 7.4E-02 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis 		12 0 1 6.7E-02 0 0
CUI: C0432230
Disease: Langer Mesomelic Dysplasia Syndrome
Langer Mesomelic Dysplasia Syndrome 		12 0 1 6.7E-02 0 0
CUI: C4024949
Disease: Generalized hyperreflexia
Generalized hyperreflexia 		12 0 1 6.7E-02 0 0
CUI: C4082769
Disease: Chronic Traumatic Encephalopathy
Chronic Traumatic Encephalopathy 		12 0 1 6.7E-02 0 0
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder) 		13 0 1 6.2E-02 0 0
CUI: C0521175
Disease: Neuropil Threads
Neuropil Threads 		13 0 1 6.2E-02 0 0
CUI: C0878486
Disease: Arteriolosclerosis
Arteriolosclerosis 		13 0 1 6.2E-02 0 0
CUI: C1861736
Disease: SPINOCEREBELLAR ATAXIA 31 (disorder)
SPINOCEREBELLAR ATAXIA 31 (disorder) 		13 0 1 6.2E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 1 6.2E-02 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 1 6.2E-02 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 5 3 6.1E-02 1 3.0E-02
CUI: C0235971
Disease: Elevated alpha-fetoprotein
Elevated alpha-fetoprotein 		14 0 1 5.9E-02 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 1 5.9E-02 0 0