Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.130 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.120 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.110 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0006131
Disease: Branchioma
Branchioma 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0013528
Disease: Echolalia
Echolalia 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0015310
Disease: Exotropia
Exotropia 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0016202
Disease: Flatfoot
Flatfoot 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0025995
Disease: Micromelia
Micromelia 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0037293
Disease: Skin tag
Skin tag 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		0.100 Biomarker HPO

Entrez Id: 22827
Gene Symbol: PUF60
PUF60
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		0.100 Biomarker HPO