Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.400 limited 1.000 0 0 2016 2016
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		disease 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1854882
Disease: Absent speech
Absent speech 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		disease 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		disease 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C0024433
Disease: Macrostomia
Macrostomia 		disease 0.100 None 0 0
Entrez Id: 80311
Gene Symbol: KLHL15
KLHL15 		kelch like family member 15 0.805 0.192 0.99
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		phenotype 0.100 None 0 1