Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0234146
Disease: Absent reflex
Absent reflex 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0158465
Disease: Acquired cubitus valgus
Acquired cubitus valgus 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0001403
Disease: Addison Disease
Addison Disease 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C1303007
Disease: Brushfield spots
Brushfield spots 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0086543
Disease: Cataract
Cataract 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		0.100 Biomarker HPO