developmental disabilities

Preferred Label : developmental disabilities;

MeSH definition : Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed);

MeSH synonym : child development disorders; development disorder, child; disabilities, developmental; development disorders, child; developmental disability; child development disorder; disability, developmental;

MeSH hyponym : child development disorders, specific; child development deviations; Developmental Delay Disorders; Developmental Delay Disorder; Child Development Deviation; Development Deviation, Child; Development Deviations, Child; Deviation, Child Development;

Wikipedia link : https://en.wikipedia.org/wiki/Developmental disabilities;

Details

Origin ID

D002658;

UMLS CUI

C0008073;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Delayed articulatory and language development (finding) [SNOMED CT concept]
- Developmental delay disorder [ICD-11 Category]
- Developmental disturbance [MedDRA LLT]
- Developmental dysfluency (disorder) [SNOMED CT concept]
- Developmental language disorder (disorder) [SNOMED CT concept]
- Developmental speech disorder (disorder) [SNOMED CT concept]
- Developmentally disabled (finding) [SNOMED CT concept]
- Failure To Thrive [ICNP diagnostic]
- Failure to Deliver [NCIt concept]
- Global developmental delay [HPO term]
- LATE DEVELOPER [WHO-ART Included Term]
- Other specified delays in development [ICD-9 code]
- Unspecified disorder of psychological development [ICD-10 category (who)]
- growth retardation [Artificial nutrition thesaurus concept]
- specific learning problem [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- DEVELOPMENTAL DELAY [WHO-ART Preferred Term]
- Developmental Delay [NCIt concept]
- Developmental Disorder [NCIt concept]
- Developmental delay [MedDRA Preferred Term]
- Developmental delay (disorder) [SNOMED CT concept]
- Developmental delay NOS [MedDRA LLT]
- Developmental disorder [PASCAL descriptor]
- Developmental disorder (disorder) [SNOMED CT concept]
- Developmental disorders [HPMULTI term]
- Developmental disorders [PASCAL theme]
- Developmental disorders [FRANCIS theme]
- Global developmental delay [HPO term]
- Unspecified delay in development [ICD-9 code]
- developmental disabilities [MedlinePlus Topic]
- developmental disorder [Radlex concept]
MedlinePlus topic(s)
- developmental disabilities [MedlinePlus Topic]
Metaterm(s)
- developmental biology and medicine [CISMeF Metaterm]
Record concept(s)
- child development deviations [MeSH concept]
- child development disorders, specific [MeSH concept]
- developmental disabilities [MeSH concept]
Related MeSH Supplementary Concept(s)
- Al Gazali Sabrinathan Nair syndrome [MeSH Supplementary Concept]
- Arginine-Glycine Amidinotransferase Deficiency [MeSH Supplementary Concept]
- Oliver-McFarlane syndrome [MeSH Supplementary Concept]
- Roifman-Chitayat syndrome [MeSH Supplementary Concept]
- Schaaf-Yang syndrome [MeSH Supplementary Concept]
- Snijders Blok-Campeau syndrome [MeSH Supplementary Concept]
- abuse dwarfism syndrome [MeSH Supplementary Concept]
- bagatelle cassidy syndrome [MeSH Supplementary Concept]
- cerebellar hypoplasia [MeSH Supplementary Concept]
- chitayat moore del bigio syndrome [MeSH Supplementary Concept]
- chitty hall webb syndrome [MeSH Supplementary Concept]
- chondrodysplasia, Megarbane-Dagher-Melki type [MeSH Supplementary Concept]
- chromosome 17p13.3 duplication syndrome [MeSH Supplementary Concept]
- chromosome 3q29 deletion syndrome [MeSH Supplementary Concept]
- chromosome Xp11.23-P11.22 duplication syndrome [MeSH Supplementary Concept]
- cohen syndrome [MeSH Supplementary Concept]
- craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation [MeSH Supplementary Concept]
- der kaloustian mcintosh silver syndrome [MeSH Supplementary Concept]
- forebrain defects [MeSH Supplementary Concept]
- fragile site 16p12 [MeSH Supplementary Concept]
- growth retardation, developmental delay, coarse facies, and early death [MeSH Supplementary Concept]
- grubben de cock borghgraef syndrome [MeSH Supplementary Concept]
- malpuech facial clefting syndrome [MeSH Supplementary Concept]
- microcephaly, growth retardation, cataract, hearing loss, and unusual appearance [MeSH Supplementary Concept]
- midface hypoplasia, obesity, developmental delay, and neonatal hypotonia [MeSH Supplementary Concept]
- myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay [MeSH Supplementary Concept]
- non-lissencephalic cortical dysplasia [MeSH Supplementary Concept]
- obesity, hyperphagia, and developmental delay [MeSH Supplementary Concept]
- partington anderson syndrome [MeSH Supplementary Concept]
- plantar lipomatosis, unusual facies, and developmental delay [MeSH Supplementary Concept]
- radioulnar synostosis, unilateral, with developmental retardation and hypotonia [MeSH Supplementary Concept]
- refsum disease with increased pipecolic acidemia [MeSH Supplementary Concept]
- succinic semialdehyde dehydrogenase deficiency [MeSH Supplementary Concept]
- ter haar syndrome [MeSH Supplementary Concept]
- tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities [MeSH Supplementary Concept]
- thumbs, stiff, with brachydactyly type A1 and developmental delay [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- child development [MeSH Descriptor]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Developmental Disorder [NCIt concept]
- Developmental disorder [PASCAL descriptor]
- Developmental disorder (disorder) [SNOMED CT concept]
- developmental disabilities [MedlinePlus Topic]
- developmental disorder [Radlex concept]
- developmental disorder, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- developmental retardation [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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