OBO ID: DOID:0110832 |
Term Name: | Usher syndrome type 1F | Search Ontology: | |
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Synonyms: |
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Definition: | An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. https://www.ncbi.nlm.nih.gov/pubmed/11398101 | ||
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Ontology: | Human Disease ( DOID:0110832 ) |
OTHER Usher syndrome type 1F PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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pcdh15buot14/uot14 | standard conditions | Miles et al., 2021 |
pcdh15buot15/uot15 | standard conditions | Miles et al., 2021 |
PHENOTYPE
No data available
CITATIONS (1)
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