OMOP Concept 4075828
Global developmental delay
StandardConditionSNOMED224958001Disorder
Maps from
6
Descendants
93
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Global developmental delay via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 156511 | Global developmental delay | Non-standard |
| HPO | HP_0001263 | Global developmental delay | Non-standard |
| Nebraska Lexicon | 224958001 | Global developmental delay | Non-standard |
| Read | E2F5.11 | Global delay | Non-standard |
| Read | Eu85.00 | [X]Global developmental delay | Non-standard |
| Read | R034y11 | [D]Global retardation | Non-standard |
Synonyms
Alternative names recorded for Global developmental delay across source vocabularies.
- Global developmental delay (disorder)
- retraso global del desarrollo
- retraso global del desarrollo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(93)Included automatically when you query with descendants.
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- 19q21.13 microdeletion syndrome
- 1Autism spectrum disorder due to AUTS2 deficiency
- 1Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
- 1Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 1Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome
- 1Basel Vanagaite Smirin Yosef syndrome
- 1CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 1CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
- 1CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome
- 1Coffin-Lowry syndrome
- 1Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome
- 1Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
- 1Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome
- 1Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
- 1Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
- 1Congenital pontocerebellar hypoplasia type 11
- 1Congenital pontocerebellar hypoplasia type 13
- 1Congenital pontocerebellar hypoplasia type 14
- 1Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency
- 1Developmental delay, facial dysmorphism syndrome due to MED13L deficiency
- 1Developmental delay with autism spectrum disorder and gait instability
- 1Early-onset epilepsy, intellectual disability, brain anomalies syndrome
- 1Early-onset obesity, hyperphagia, severe developmental delay syndrome
- 1Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
- 1Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome
- 1Fatty acyl-CoA reductase 1 deficiency
- 1Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
- 1Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome
- 1Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
- 1Global developmental delay, osteopenia, ectodermal defect syndrome
- 1Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
- 1Growth retardation, mild developmental delay, chronic hepatitis syndrome
- 1Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
- 1Infantile multisystem neurologic, endocrine, pancreatic disease
- 1Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome
- 1Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
- 1Intellectual disability, early-onset cataract, microcephaly syndrome
- 1Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome
- 1Intellectual disability, hyperkinetic movement, truncal ataxia syndrome
- 1Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome
- 1Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome
- 1Intellectual disability, severe speech delay, mild dysmorphism syndrome
- 1ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
- 1Lamb Shaffer syndrome
- 1Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
- 1Megaconial congenital muscular dystrophy
- 1Megalencephaly, severe kyphoscoliosis, overgrowth syndrome
- 1Microcephalic cortical malformations, short stature due to RTTN deficiency
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