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: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C2931010
Disease: Congenital disorder of glycosylation type 2E
Congenital disorder of glycosylation type 2E 		disease 0.600 None 1.000 0 4 2004 2016
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1446712
Disease: Overlapping fingers
Overlapping fingers 		disease 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		phenotype 0.100 None 0 2
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C0521525
Disease: Short neck
Short neck 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C0426421
Disease: Wide nose
Wide nose 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1844909
Disease: Recurrent infections in infancy and early childhood
Recurrent infections in infancy and early childhood 		phenotype 0.100 None 0 2
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C4023343
Disease: Nasogastric tube feeding in infancy
Nasogastric tube feeding in infancy 		phenotype 0.100 None 0 2
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		phenotype 0.100 None 0 2
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		disease 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C3494422
Disease: Retrognathia
Retrognathia 		disease 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C2749688
Disease: Abnormal isoelectric focusing of serum transferrin
Abnormal isoelectric focusing of serum transferrin 		phenotype 0.100 None 0 2
Entrez Id: 91949
Gene Symbol: COG7
COG7 		component of oligomeric golgi complex 7 0.686 0.500 2.6E-07
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		disease 0.100 None 0 2