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.
推出的年份: 2006
树号: 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
MeSH 单一 ID: D052245
进入的组:
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 3
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 IId
早前的内容:
Deafness (1972-2005)
Hearing Loss, Sensorineural (1983-2005)
Retinitis Pigmentosa (1972-2005)
Syndrome (1972-2005)
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