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Achromatopsia
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Myopathy Superpanel
NCGC
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Prepair 1000+
Prepair 500+
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Retinitis Pigmentosa Superpanel
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Severe Combined Immunodeficiency (absent T present B cells)
Severe early-onset obesity
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Sick sinus syndrome
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Stickler Syndrome
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TCGA_PANCAN_2018
Transplant Co-Morbidity Superpanel
Tremors_Superpanel
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
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Usher Syndrome
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Vascular Malformations SuperPanel
Vasculitis
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Wilms Tumour Predisposition
Version
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0.2
Gene or Genomic Entity Name
EGFR
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07 Jan 2020
CGC_86 v0.0
EGFR
Lavinia Gordon gene: EGFR was added
gene: EGFR was added to CGC_86. Sources: CGC_86
Mode of inheritance for gene: EGFR was set to Other
Phenotypes for gene: EGFR were set to NA