- 1. Xeroderma
- (UMLS (NCI) C0043345) =Disease or Syndrome
| - 7. Xeroderma Pigmentosum Complementation Group F
- (UMLS (NCI) C0268140) =Congenital Abnormality; Disease or Syndrome
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- 2. XERODERMA OF EYELID
- [ ] (UMLS (ICD9CM) C0155179) =Disease or Syndrome ;
| - 8. Xeroderma Pigmentosum Complementation Group G
- (UMLS (NCI) C0268141) =Congenital Abnormality; Disease or Syndrome
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- 3. Xeroderma Pigmentosum Complementation Group A
- (UMLS (NCI) C0268135) =Congenital Abnormality; Disease or Syndrome
| - 9. Xeroderma Pigmentosum, Complementation Group A Gene
- [This gene facilitates DNA binding in repair processes and is associated with the disease xeroderma pigmentosum complementation group A. ( NCI )] (UMLS (NCI) C1337030) XPA;
XPA Gene =Gene or Genome ;
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- 4. Xeroderma Pigmentosum Complementation Group A Protein
- [DNA-Repair Protein Complementing XP-A Cells (XPA), the nuclear protein encoded by the XPA gene, has a zinc finger domain and is involved in the DNA excision repair pathway. XPA initiates repair by binding to damaged sites with various affinities, depending on the photoproduct and the transcriptional state of the region. XPA complements the defect in xeroderma pigmentosum (XP) group A (XP-A), an autosomal recessive disease characterized by hypersensitivity of the skin to sunlight followed by high incidence of skin cancer and frequent neurologic abnormalities. Group A patients show the most severe skin symptoms and progressive neurological disorders. ( NCI )] (UMLS (NCI) C1506533) Xeroderma Pigmentosum Group A Complementing Protein;
XPA =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
| - 10. xerography
- [(ZEE-ro-ray-dee-AH-gra-fee) A type of x-ray in which a picture of the body is recorded on paper rather than on film. ( NCI )] (UMLS (CSP) C0043350) =Diagnostic Procedure
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- 5. Xeroderma Pigmentosum Complementation Group B
- (UMLS (NCI) C0268136) =Congenital Abnormality; Disease or Syndrome
| - 11. xerotic keratitis
- [ ] (UMLS (CSP) C0271271) =Disease or Syndrome
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- 6. Xeroderma Pigmentosum Complementation Group D
- (UMLS (NCI) C0268138) =Congenital Abnormality; Disease or Syndrome
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