SOD1, superoxide dismutase 1, 6647

N. diseases: 689; N. variants: 68
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.800 Biomarker disease HPO
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.620 Biomarker disease HPO
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		0.430 Biomarker phenotype HPO
CUI: C3542025
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.300 CausalMutation disease CLINVAR
CUI: C0013238
Disease: Dry Eye Syndromes
Dry Eye Syndromes 		0.210 Biomarker disease MGD
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		0.170 Biomarker phenotype HPO
CUI: C0030193
Disease: Pain
Pain 		0.150 Biomarker phenotype HPO
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		0.130 Biomarker phenotype HPO
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.130 Biomarker phenotype HPO
CUI: C0003467
Disease: Anxiety
Anxiety 		0.120 Biomarker disease HPO
CUI: C0015672
Disease: Fatigue
Fatigue 		0.120 Biomarker phenotype HPO
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure 		0.120 Biomarker disease HPO
CUI: C0085633
Disease: Mood swings
Mood swings 		0.110 Biomarker disease HPO
CUI: C0013404
Disease: Dyspnea
Dyspnea 		0.100 Biomarker phenotype HPO
CUI: C0023066
Disease: Laryngospasm
Laryngospasm 		0.100 Biomarker disease HPO
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting 		0.100 Biomarker phenotype HPO
CUI: C0033790
Disease: Pseudobulbar Palsy
Pseudobulbar Palsy 		0.100 Biomarker disease HPO
CUI: C0037315
Disease: Sleep Apnea Syndromes
Sleep Apnea Syndromes 		0.100 Biomarker disease HPO
CUI: C0037763
Disease: Spasm
Spasm 		0.100 Biomarker phenotype HPO
CUI: C0043352
Disease: Xerostomia
Xerostomia 		0.100 Biomarker disease HPO
CUI: C0085631
Disease: Agitation
Agitation 		0.100 Biomarker phenotype HPO
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		0.100 Biomarker phenotype HPO
CUI: C0522224
Disease: Paralysed
Paralysed 		0.100 Biomarker phenotype HPO
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		0.100 Biomarker phenotype HPO
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		0.100 Biomarker phenotype HPO