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Achromatopsia
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Prepair 1000+
Prepair 500+
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Retinitis Pigmentosa Superpanel
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Stickler Syndrome
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TCGA_PANCAN_2018
Transplant Co-Morbidity Superpanel
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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
XPA
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07 Jan 2020
NCGC v0.0
XPA
Lavinia Gordon gene: XPA was added
gene: XPA was added to NCGC. Sources: NCGC
Mode of inheritance for gene: XPA was set to Other
Phenotypes for gene: XPA were set to Xeroderma pigmentosum, type 1