"Usher Syndromes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.
- Usher Syndromes
- Syndrome, Usher
- Syndromes, Usher
- Usher Syndrome
- Retinitis Pigmentosa-Deafness Syndrome
- Retinitis Pigmentosa Deafness Syndrome
- Retinitis Pigmentosa-Deafness Syndromes
- Syndrome, Retinitis Pigmentosa-Deafness
- Syndromes, Retinitis Pigmentosa-Deafness
Usher Syndrome, Type I
- Usher Syndrome, Type I
- Usher Syndrome, Type I, French Variety
- Usher Syndrome, Type 1A
- Retinitis Pigmentosa And Congenital Deafness
- Usher Syndrome, Type 1
Below are MeSH descriptors whose meaning is more general than "Usher Syndromes".
Below are MeSH descriptors whose meaning is more specific than "Usher Syndromes".
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