Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine
0.200 Biomarker group MGD
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
0.200 GeneticVariation disease CLINVAR
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
0.200 Biomarker disease HPO
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia
0.200 Biomarker disease MGD
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia
0.200 Biomarker disease HPO
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC
0.180 CausalMutation disease CLINVAR
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
0.170 Biomarker disease HPO
CUI: C0018991
Disease: Hemiplegia
Hemiplegia
0.140 Biomarker phenotype HPO
CUI: C0040485
Disease: Torticollis
Torticollis
0.140 Biomarker phenotype HPO
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
0.140 Biomarker group HPO
CUI: C0015967
Disease: Fever
Fever
0.130 Biomarker phenotype HPO
CUI: C0042571
Disease: Vertigo
Vertigo
0.130 Biomarker phenotype HPO
CUI: C0042571
Disease: Vertigo
Vertigo
0.130 GeneticVariation phenotype CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.130 GeneticVariation disease CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.130 Biomarker disease HPO
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
0.130 GeneticVariation phenotype CLINVAR
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.120 Biomarker disease HPO
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
0.120 Biomarker phenotype HPO
CUI: C1836830
Disease: Developmental regression
Developmental regression
0.120 Biomarker disease HPO
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.120 Biomarker group HPO
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.110 Biomarker disease HPO
CUI: C0009421
Disease: Comatose
Comatose
0.110 Biomarker phenotype HPO
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.110 Biomarker group HPO
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
0.110 Biomarker disease HPO
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
0.110 Biomarker phenotype HPO