"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 |
|---|
| 1996 | 5 | 1 | 6 |
| 1997 | 0 | 1 | 1 |
| 1998 | 5 | 1 | 6 |
| 1999 | 2 | 2 | 4 |
| 2000 | 5 | 0 | 5 |
| 2001 | 3 | 1 | 4 |
| 2002 | 6 | 1 | 7 |
| 2003 | 4 | 2 | 6 |
| 2004 | 3 | 4 | 7 |
| 2005 | 8 | 4 | 12 |
| 2006 | 6 | 2 | 8 |
| 2007 | 12 | 3 | 15 |
| 2008 | 3 | 3 | 6 |
| 2009 | 6 | 3 | 9 |
| 2010 | 7 | 4 | 11 |
| 2011 | 6 | 2 | 8 |
| 2012 | 10 | 9 | 19 |
| 2013 | 10 | 5 | 15 |
| 2014 | 8 | 1 | 9 |
| 2015 | 11 | 0 | 11 |
| 2016 | 21 | 5 | 26 |
| 2017 | 18 | 5 | 23 |
| 2018 | 16 | 8 | 24 |
| 2019 | 25 | 8 | 33 |
| 2020 | 23 | 8 | 31 |
| 2021 | 32 | 8 | 40 |
| 2022 | 32 | 1 | 33 |
| 2023 | 30 | 0 | 30 |
| 2024 | 13 | 11 | 24 |
| 2025 | 11 | 4 | 15 |
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Below are the most recent publications written about "Intellectual Disability" by people in Profiles.
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Longitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study. Pediatr Neurol. 2026 Feb; 175:8-18.
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Innovative Web-Based Future Planning and Well-Being for Caregivers of Individuals With Intellectual and Developmental Disabilities: Protocol of a Pragmatic Randomized Controlled Trial. JMIR Res Protoc. 2025 Oct 01; 14:e77184.
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Intellectual and Neurodevelopmental Delays in Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: Distinct Characteristics and a More Malignant Neurocardiac Phenotype. Circ Arrhythm Electrophysiol. 2025 Oct; 18(10):e013437.
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De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder. Am J Med Genet A. 2026 Jan; 200(1):244-252.
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Case Series of Nizon-Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid-Triploid Mosaicism. Am J Med Genet A. 2026 Jan; 200(1):205-214.
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Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures. Am J Hum Genet. 2025 Jul 03; 112(7):1722-1732.
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Evaluating the consistency of SMARCB1 variant classification and assertions of genotype-phenotype relationships in ClinVar. Cancer Genet. 2025 Sep; 296-297:84-87.
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Rest-activity rhythm phenotypes in adults with epilepsy and intellectual disability. Epilepsia Open. 2025 Aug; 10(4):1086-1098.
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Biallelic MED16 variants disrupt neural development and lead to an intellectual disability syndrome. J Genet Genomics. 2025 10; 52(10):1189-1198.
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Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder. Am J Hum Genet. 2025 May 01; 112(5):1117-1138.