OBO ID: DOID:0111405 |
Term Name: | Fraser syndrome 1 | Search Ontology: | |
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Synonyms: |
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Definition: | A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21.21. https://www.ncbi.nlm.nih.gov/pubmed/12766769 | ||
References: | |||
Ontology: | Human Disease ( DOID:0111405 ) |
OTHER Fraser syndrome 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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