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Usher Syndromes
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate concepts∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate concepts∟ ∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes 4 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Usher Syndromes ∟ ∟ ∟ ∟ Usher Syndromes ∟ ∟ ∟ ∟ ∟ Usher Syndromes ∟ ∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes ∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Usher Syndromes |
History note: | Deafness (1972-2005) | Hearing Loss, Sensorineural (1983-2005) | Retinitis Pigmentosa (1972-2005) | Syndrome (1972-2005)X |
historyNote*: | 2006
X |
publicMeSHNote*: | 2006
X |
Scope note: | 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.
X |
activeMeSHYear*: | |
dateCreated*: | 2005-06-30X |
dateEstablished*: | 2006-01-01X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | nnsX |
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Labels and equivalent concepts: | Usher-oireyhtymät (fi) XUsher Syndrome (en, replaced) Síndromes de Usher (es) Usher-Syndrome (de) Usherovy syndromy (cs) Usher-Syndrom, Typ II (de, replaced) Usher-Syndrom, Typ III (de, replaced) Usher-Syndrom, Typ I (de, replaced) Usherův syndrom - typ III (cs, replaced) Usherův syndrom - typ I (cs, replaced) Usherův syndrom - typ II (cs, replaced) Usherův syndrom (cs, replaced) |
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