Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.110 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0003578
Disease: Apnea
Apnea
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0004096
Disease: Asthma
Asthma
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0014877
Disease: Esotropia
Esotropia
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
Sensorineural Hearing Loss (disorder)
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0022346
Disease: Icterus
Icterus
0.100 Biomarker HPO