Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Obesity, Hyperphagia, and Developmental Delay
0.700 Biomarker disease CTD_human
Obesity, Hyperphagia, and Developmental Delay
0.700 CausalMutation disease CLINVAR
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58
0.600 GeneticVariation disease CLINVAR
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58
0.600 CausalMutation disease CLINVAR
CUI: C0028754
Disease: Obesity
Obesity
0.440 Biomarker disease HPO
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.410 Biomarker disease HPO
CUI: C0020505
Disease: Hyperphagia
Hyperphagia
0.400 Biomarker phenotype HPO
CUI: C0037769
Disease: West Syndrome
West Syndrome
0.400 Biomarker disease HPO
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus
0.400 Biomarker disease HPO
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.350 GeneticVariation disease UNIPROT
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.320 GeneticVariation disease UNIPROT
CUI: C0036572
Disease: Seizures
Seizures
0.110 GeneticVariation phenotype CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.110 GeneticVariation disease CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.110 Biomarker disease HPO
Attention deficit hyperactivity disorder
0.110 Biomarker disease HPO
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype HPO
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
0.100 Biomarker disease HPO
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker disease HPO
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
0.100 Biomarker disease HPO
CUI: C0018552
Disease: Hamartoma
Hamartoma
0.100 GeneticVariation disease CLINVAR
CUI: C0018681
Disease: Headache
Headache
0.100 GeneticVariation phenotype CLINVAR
CUI: C0020608
Disease: Hypodontia
Hypodontia
0.100 Biomarker disease HPO
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
0.100 Biomarker phenotype HPO