Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C4479520
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES 		0.700 GeneticVariation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C4479520
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES 		0.700 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0036572
Disease: Seizures
Seizures 		0.110 GeneticVariation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0036572
Disease: Seizures
Seizures 		0.110 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0036572
Disease: Seizures
Seizures 		0.110 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.110 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.110 GeneticVariation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.100 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.100 GeneticVariation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		0.100 GeneticVariation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		0.100 Biomarker HPO