OBO ID: DOID:0080040 |
Term Name: | fibrogenesis imperfecta ossium | Search Ontology: | |
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Definition: | A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures. https://www.ncbi.nlm.nih.gov/pubmed/7559718 | ||
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Ontology: | Human Disease ( DOID:0080040 ) |
OTHER fibrogenesis imperfecta ossium PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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