Deficient excision of UV-induced pyrimidine dimers in DNA
Symptom Information:
Symptom ID: | HPO:0003213 | ||||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of nucleobase metabolism(HPO:0010932) Abnormality of pyrimidine metabolism(HPO:0004353) Deficient excision of UV-induced pyrimidine dimers in DNA(HPO:0003213) Abnormality of cell physiology(HPO:0011017) Abnormality of DNA repair(HPO:0003254) Deficient excision of UV-induced pyrimidine dimers in DNA(HPO:0003213) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
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All diseases associated with this symptom:
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
Fanconi anemia | (Orphanet:84) |