OBO ID: DOID:0111092 |
Term Name: | Fanconi anemia complementation group P | Search Ontology: | |
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Synonyms: |
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Definition: | A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3. (2) | ||
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Ontology: | Human Disease ( DOID:0111092 ) |
OTHER Fanconi anemia complementation group P PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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