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Retinal degeneration associated with rhodopsin mutations
retinitis pigmentosa that has material basis in mutation in the RHO gene on chromosome 3q22
Pronunciation
/ˈrɛtnəl dəˌʤɛnəˈreɪʃən əˈsoʊsiˌeɪdɪd wɪθ roʊˈdɑpsən mjuˈteɪʃənz/
/ˈrɛtɪnəl dɪˌʤɛnəˈreɪʃən əˈsəʊʃɪeɪtɪd wɪð rəʊˈdɒpsɪn mjuːˈteɪʃənz/
Categories
autosomal recessive disease
genetic disease
retinal degeneration
retinitis pigmentosa
rare disease