Stereotypy associated with neurodevelopmental disorders (Q85466): Difference between revisions
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A estereotipia refere-se a movimentos simples ou complexos que se repetem continuamente e de forma idêntica. Geralmente não são precedidos por uma sensação desconfortável. A estereotipia pode estar associada a transtorno do neurodesenvolvimento, como transtorno do espectro autista, incapacidade intelectual, síndromes genéticas e deficiência sensorial. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Stereotypy refers to simple or complex movements that repeat themselves continually and identically. These are usually not preceded by an uncomfortable feeling. Stereotypy can be associated with neurodevelopmental disorders such as autistic spectrum disorder, intellectual disabilities, genetic syndromes, and sensory impairment. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1694934550 / rank | |||||||||||||||
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CID11:ID_1694934550 | |||||||||||||||
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dki-india-ID_1694934550 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 10:49, 15 August 2026
Stereotypy refers to simple or complex movements that repeat themselves continually and identically. These are usually not preceded by an uncomfortable feeling. Stereotypy can be associated with neurodevelopmental disorders such as autistic spectrum disorder, intellectual disabilities, genetic syndromes, and sensory impairment.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1694934550 |
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| English | Stereotypy associated with neurodevelopmental disorders |
Stereotypy refers to simple or complex movements that repeat themselves continually and identically. These are usually not preceded by an uncomfortable feeling. Stereotypy can be associated with neurodevelopmental disorders such as autistic spectrum disorder, intellectual disabilities, genetic syndromes, and sensory impairment. |
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CID11:ID_1694934550
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dki-india-ID_1694934550
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Concluído
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13 August 2026
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