"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 |
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1997 | 1 | 1 | 2 |
1998 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2002 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2006 | 0 | 2 | 2 |
2007 | 2 | 1 | 3 |
2009 | 1 | 0 | 1 |
2010 | 3 | 1 | 4 |
2011 | 4 | 2 | 6 |
2012 | 8 | 1 | 9 |
2013 | 11 | 0 | 11 |
2014 | 5 | 1 | 6 |
2015 | 6 | 0 | 6 |
2016 | 5 | 3 | 8 |
2017 | 7 | 2 | 9 |
2018 | 7 | 1 | 8 |
2019 | 4 | 0 | 4 |
2020 | 7 | 0 | 7 |
2021 | 8 | 0 | 8 |
2022 | 4 | 0 | 4 |
2023 | 3 | 0 | 3 |
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Below are the most recent publications written about "Intellectual Disability" by people in Profiles.
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The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder. Am J Hum Genet. 2023 06 01; 110(6):963-978.
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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant. Eur J Hum Genet. 2023 04; 31(4):461-468.
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Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype. Cells. 2023 01 05; 12(2).
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Genetic (Re-)evaluation to Optimize the Care of Adults With Intellectual Disability. Dtsch Arztebl Int. 2022 12 27; 119(51-52):895-896.
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Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications. Brain. 2022 09 14; 145(9):2991-3009.
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ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model. Am J Hum Genet. 2022 08 04; 109(8):1436-1457.
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Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes (Basel). 2022 02 25; 13(3).
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TP63-related disorders: two case reports and a brief review of the literature. Dermatol Online J. 2021 Nov 15; 27(11).
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A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes (Basel). 2021 09 24; 12(10).
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Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. Eur J Hum Genet. 2021 11; 29(11):1663-1668.