OBO ID: DOID:0110827 |
Term Name: | Usher syndrome type 2 | Search Ontology: | |
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Synonyms: |
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Definition: | An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa. (4) | ||
References: |
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Ontology: | Human Disease ( DOID:0110827 ) |
OTHER Usher syndrome type 2 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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ush2ahzu6/hzu6 | standard conditions | Han et al., 2018 |
PHENOTYPE
No data available
CITATIONS (1)
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