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: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0268540
Disease: HHH syndrome
HHH syndrome 		disease 0.800 None 0.952 7 18 1999 2016
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		phenotype 0.130 None 1.000 0 0 1999 2004
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0599035
Disease: Hyperornithinemia
Hyperornithinemia 		phenotype 0.120 None 1.000 0 0 2001 2010
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1833434
Disease: Multifocal cerebral white matter abnormalities
Multifocal cerebral white matter abnormalities 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1306587
Disease: Acute encephalopathy
Acute encephalopathy 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0563243
Disease: Poor coordination
Poor coordination 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0424230
Disease: Motor retardation
Motor retardation 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1839531
Disease: Protein avoidance
Protein avoidance 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4022483
Disease: Chorioretinal hypopigmentation
Chorioretinal hypopigmentation 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4021761
Disease: Morphological abnormality of the pyramidal tract
Morphological abnormality of the pyramidal tract 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		phenotype 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		disease 0.100 None 0 0
Entrez Id: 10166
Gene Symbol: SLC25A15
SLC25A15 		solute carrier family 25 member 15 0.711 0.346 3.7E-07
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		phenotype 0.100 None 0 0