Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1290508
Disease: Abnormal number of teeth
Abnormal number of teeth 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		0.120 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.120 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1442965
Disease: Avascular necrosis of the capital femoral epiphysis
Avascular necrosis of the capital femoral epiphysis 		0.110 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1850327
Disease: Bifid uterus
Bifid uterus 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.110 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1867131
Disease: Broad hallux
Broad hallux 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0086543
Disease: Cataract
Cataract 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1857627
Disease: Chorioretinal dystrophy
Chorioretinal dystrophy 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0266292
Disease: Congenital anomaly of the kidney
Congenital anomaly of the kidney 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0265563
Disease: Congenital dislocation of radial head
Congenital dislocation of radial head 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		0.100 Biomarker HPO

Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO