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: C0001403
Disease: Addison Disease
Addison Disease 		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: C0004134
Disease: Ataxia
Ataxia 		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: C0008925
Disease: Cleft Palate
Cleft Palate 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0013362
Disease: Dysarthria
Dysarthria 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0020757
Disease: Ichthyoses
Ichthyoses 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0022346
Disease: Icterus
Icterus 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome 		0.100 Biomarker HPO

Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker HPO