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: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
Abnormality of cardiovascular system morphology 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0234146
Disease: Absent reflex
Absent reflex 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0158465
Disease: Acquired cubitus valgus
Acquired cubitus valgus 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		0.100 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: C0238621
Disease: Aminoaciduria
Aminoaciduria 		0.100 Biomarker HPO

Entrez Id: 5830
Gene Symbol: PEX5
PEX5
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		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: 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: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		0.100 Biomarker HPO