[Senear-Usher syndrome]. 1951

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UI MeSH Term Description Entries
D010392 Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. Pemphigus Vulgaris,Pemphigus Foliaceus,Foliaceus, Pemphigus
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D052245 Usher Syndromes 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. Deafness-Retinitis Pigmentosa Syndrome,Dystrophia Retinae Pigmentosa-Dysostosis Syndrome,Graefe-Usher Syndrome,Hallgren Syndrome,Retinitis Pigmentosa And Congenital Deafness,Retinitis Pigmentosa-Deafness Syndrome,Usher Syndrome,Usher Syndrome, Type 1,Usher Syndrome, Type 1A,Usher Syndrome, Type 3,Usher Syndrome, Type I,Usher Syndrome, Type I, French Variety,Usher Syndrome, Type II,Usher Syndrome, Type III,Usher Syndrome, Type IId,Usher's Syndrome,Deafness Retinitis Pigmentosa Syndrome,Deafness-Retinitis Pigmentosa Syndromes,Dystrophia Retinae Pigmentosa Dysostosis Syndrome,Graefe Usher Syndrome,Pigmentosa Syndromes, Deafness-Retinitis,Retinitis Pigmentosa Deafness Syndrome,Retinitis Pigmentosa-Deafness Syndromes,Syndrome, Deafness-Retinitis Pigmentosa,Syndrome, Graefe-Usher,Syndrome, Hallgren,Syndrome, Retinitis Pigmentosa-Deafness,Syndrome, Usher,Syndrome, Usher's,Syndromes, Deafness-Retinitis Pigmentosa,Syndromes, Retinitis Pigmentosa-Deafness,Syndromes, Usher,Ushers Syndrome

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