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.

Descriptor ID	D052245
MeSH Number(s)	C09.218.458.341.186.500.500 C09.218.458.341.887.886 C10.597.751.418.341.186.500.500 C10.597.751.418.341.887.886 C10.597.751.941.162.625.500 C11.768.585.658.500.813 C11.966.075.375.500 C16.131.077.299.500 C16.320.290.684.500 C23.888.592.763.393.341.887.886
Concept/Terms	Usher Syndromes Usher Syndromes Syndrome, Usher Syndromes, Usher Usher Syndrome Usher's Syndrome Syndrome, Usher's Ushers Syndrome Dystrophia Retinae Pigmentosa-Dysostosis Syndrome Dystrophia Retinae Pigmentosa Dysostosis Syndrome Graefe-Usher Syndrome Graefe Usher Syndrome Syndrome, Graefe-Usher Hallgren Syndrome Syndrome, Hallgren Retinitis Pigmentosa-Deafness Syndrome Retinitis Pigmentosa Deafness Syndrome Retinitis Pigmentosa-Deafness Syndromes Syndrome, Retinitis Pigmentosa-Deafness Syndromes, Retinitis Pigmentosa-Deafness Deafness-Retinitis Pigmentosa Syndrome Deafness Retinitis Pigmentosa Syndrome Deafness-Retinitis Pigmentosa Syndromes Pigmentosa Syndromes, Deafness-Retinitis Syndrome, Deafness-Retinitis Pigmentosa Syndromes, Deafness-Retinitis Pigmentosa Usher Syndrome, Type III Usher Syndrome, Type III Usher Syndrome, Type 3 Usher Syndrome, Type I Usher Syndrome, Type I Usher Syndrome, Type 1A Retinitis Pigmentosa And Congenital Deafness Usher Syndrome, Type 1 Usher Syndrome, Type I, French Variety Usher Syndrome, Type II Usher Syndrome, Type II Usher Syndrome, Type IId

Below are MeSH descriptors whose meaning is more general than "Usher Syndromes".

Below are MeSH descriptors whose meaning is related to "Usher Syndromes".

Below are MeSH descriptors whose meaning is more specific than "Usher Syndromes".