Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.120 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0009024
Disease: Clonus
Clonus 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0152421
Disease: Macrotia
Macrotia 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C1855285
Disease: Protruding ear
Protruding ear 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C3279322
Disease: Progressive flexion contractures
Progressive flexion contractures 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		0.100 Biomarker HPO

Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		0.100 Biomarker HPO