Chromosomal breakage induced by crosslinking agents
Symptom Information:
Symptom ID: | HPO:0003221 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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 cell physiology(HPO:0011017) Abnormality of chromosome stability(HPO:0003220) Chromosomal breakage induced by crosslinking agents(HPO:0003221) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
FANCONI ANEMIA, COMPLEMENTATION GROUP I | (OMIM:609053) |
FANCONI ANEMIA, COMPLEMENTATION GROUP J | (OMIM:609054) |
FANCONI ANEMIA, COMPLEMENTATION GROUP N | (OMIM:610832) |
Fanconi anemia | (Orphanet:84) |
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations | (Orphanet:319462) |