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: C3151343
Disease: SPINOCEREBELLAR ATAXIA 32
SPINOCEREBELLAR ATAXIA 32 		2 0 2 0.12 0 0
CUI: C0032586
Disease: Polyradiculopathy
Polyradiculopathy 		3 0 2 0.12 0 0
CUI: C0392185
Disease: Verbal repetition
Verbal repetition 		3 0 2 0.12 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia 		4 0 2 0.11 0 0
CUI: C1837728
Disease: AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder) 		4 0 2 0.11 0 0
CUI: C1848922
Disease: Hexosaminidase alpha-Subunit Deficiency (Variant B)
Hexosaminidase alpha-Subunit Deficiency (Variant B) 		4 0 2 0.11 0 0
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY 		4 0 2 0.11 0 0
CUI: C2146481
Disease: Bilateral vocal cord paralysis
Bilateral vocal cord paralysis 		4 0 2 0.11 0 0
CUI: C4021580
Disease: Progressive extrapyramidal muscular rigidity
Progressive extrapyramidal muscular rigidity 		4 0 2 0.11 0 0
CUI: C0039373
Disease: Tay-Sachs Disease
Tay-Sachs Disease 		26 0 4 0.11 0 0
CUI: C0282550
Disease: Persian Gulf Syndrome
Persian Gulf Syndrome 		5 0 2 0.11 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive 		5 0 2 0.11 0 0
CUI: C1142448
Disease: Apraxia of eyelid
Apraxia of eyelid 		5 0 2 0.11 0 0
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
Stereotyped behavior (Psychiatry) 		5 0 2 0.11 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 5 9.8E-02 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 3 9.7E-02 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 2 9.5E-02 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 2 9.1E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 3 8.8E-02 0 0
CUI: C0043121
Disease: Wernicke Encephalopathy
Wernicke Encephalopathy 		9 0 2 8.7E-02 0 0
CUI: C1847651
Disease: Rapidly progressive dementia
Rapidly progressive dementia 		9 0 2 8.7E-02 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 4 8.5E-02 0 0
CUI: C0030442
Disease: Progressive bulbar palsy
Progressive bulbar palsy 		10 0 2 8.3E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 2 8.3E-02 0 0
CUI: C0241423
Disease: Atrophy of tongue
Atrophy of tongue 		10 0 2 8.3E-02 0 0