Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		0.400 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0014877
Disease: Esotropia
Esotropia 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0015310
Disease: Exotropia
Exotropia 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0151526
Disease: Premature Birth
Premature Birth 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0240953
Disease: Winged scapula
Winged scapula 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0349588
Disease: Short stature
Short stature 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0423848
Disease: Distichiasis
Distichiasis 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C1854301
Disease: Motor delay
Motor delay 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C1866933
Disease: Structural brain abnormalities
Structural brain abnormalities 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C4022727
Disease: Stellate iris
Stellate iris 		0.100 CausalMutation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		0.100 CausalMutation CLINVAR