"Intellectual Disability" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)
| Descriptor ID |
D008607
|
| MeSH Number(s) |
C10.597.606.643 C23.888.592.604.646 F01.700.687 F03.625.539
|
| Concept/Terms |
Intellectual Disability- Intellectual Disability
- Disabilities, Intellectual
- Intellectual Disabilities
- Retardation, Mental
- Mental Retardation
- Disability, Intellectual
- Intellectual Development Disorder
- Development Disorder, Intellectual
- Development Disorders, Intellectual
- Disorder, Intellectual Development
- Disorders, Intellectual Development
- Intellectual Development Disorders
Mental Retardation, Psychosocial- Mental Retardation, Psychosocial
- Mental Retardations, Psychosocial
- Psychosocial Mental Retardation
- Psychosocial Mental Retardations
- Retardation, Psychosocial Mental
- Retardations, Psychosocial Mental
Deficiency, Mental- Deficiency, Mental
- Deficiencies, Mental
- Mental Deficiencies
- Mental Deficiency
|
Below are MeSH descriptors whose meaning is more general than "Intellectual Disability".
Below are MeSH descriptors whose meaning is more specific than "Intellectual Disability".
This graph shows the total number of publications written about "Intellectual Disability" by people in this website by year, and whether "Intellectual Disability" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 3 | 0 | 3 |
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 1 | 2 |
| 1998 | 1 | 0 | 1 |
| 1999 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 2 | 3 |
| 2005 | 1 | 0 | 1 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 2 | 1 | 3 |
| 2009 | 1 | 1 | 2 |
| 2010 | 3 | 0 | 3 |
| 2011 | 3 | 1 | 4 |
| 2012 | 1 | 2 | 3 |
| 2013 | 4 | 0 | 4 |
| 2014 | 3 | 2 | 5 |
| 2015 | 2 | 1 | 3 |
| 2016 | 5 | 2 | 7 |
| 2017 | 3 | 0 | 3 |
| 2018 | 2 | 0 | 2 |
| 2019 | 3 | 1 | 4 |
| 2020 | 2 | 0 | 2 |
| 2021 | 5 | 2 | 7 |
| 2022 | 3 | 0 | 3 |
| 2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Intellectual Disability" by people in Profiles.
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Types and correlates of school absenteeism among students with intellectual disability. J Intellect Disabil Res. 2023 04; 67(4):375-386.
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Relationship of Nonsteroidal Anti-Inflammatory Drug Use During Pregnancy with Autism Spectrum Disorder and Intellectual Disability Among Offspring. J Womens Health (Larchmt). 2023 Mar; 32(3):356-365.
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Social and community inclusion outcomes for adults with autism with and without intellectual disability in Australia. J Intellect Disabil Res. 2022 07; 66(7):655-666.
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Clinical findings from the landmark MEF2C-related disorders natural history study. Mol Genet Genomic Med. 2022 06; 10(6):e1919.
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Emanuel syndrome and congenital diaphragmatic hernia: A systematic review. J Pediatr Surg. 2022 Sep; 57(9):24-28.
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Developing Freely Accessible Educational Videos to Enhance Knowledge of Autism Spectrum Disorder and Intellectual Disability. J Am Acad Child Adolesc Psychiatry. 2022 01; 61(1):1-2.
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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism. Am J Hum Genet. 2021 06 03; 108(6):1138-1150.
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Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities. Cell Rep Med. 2021 04 20; 2(4):100240.
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Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Sci Transl Med. 2021 02 10; 13(580).
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Atypical aplasia cutis in association with Xia Gibbs syndrome. Pediatr Dermatol. 2021 Mar; 38(2):533-535.