Global developmental delay
Basic details
Preferred term: Global developmental delay
Alt. terms: Cognitive delay | Delayed cognitive development | Delayed development | Delayed developmental milestones | Delayed intellectual development | Delayed milestones | Delayed psychomotor development | Developmental delay | Developmental delay in early ch
HPO term: Global developmental delay
HPO code: HP:0001263
GenIA ID: 1779
Last updated on: 2021-08-02 21:50:33
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -
Description
A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age. Note: Developmental retardation is any significant lag in development in the any or all of the physical, cognitive, behavioral, emotional, or social spheres. Note that the term intellectual disability (mental retardation) refers to not merely a delay in development but rather a permanent limitation. Note that the term 'psychomotor retardation' is also used in some contexts to refer to a slowing of thought and physical movements as a result of major depression or intoxication.
Hierarchical classification
PARENT terms
TERM
Global developmental delay
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
102313 | M | 214935![]() |
- | Turkish | Neurodevelopmental delay | Otofaciocervical syndrome 2 | PMID:23851939 [V-2(V.2)] |
102353 | M | 214936![]() |
- | Indian | Neurodevelopmental delay | Otofaciocervical syndrome 2 | PMID:29681087 [P1(II.1)] |
102356 | F | 214936![]() |
- | Indian | Neurodevelopmental delay | Otofaciocervical syndrome 2 | PMID:29681087 [Fam.P1:II.2(P2)] |
102410 | F | 214947![]() |
2 | South Asian | Global developmental delay | Hyper-IgE recurrent infection syndrome 4B | PMID:28747427 [Fam.A:II.3(P1)] |
102419 | M | 214948![]() |
- | Irish Traveller | Global developmental delay | Immunodeficiency 54 | PMID:16532402 [Fam.A:IV.8(P1)]; PMID:22354167 [Fam.A:IV.8(P1.1)] |
102433 | M | 214951![]() |
- | Irish Traveller | Global developmental delay | Immunodeficiency 54 | PMID:22354167 [Fam.B:II.1(P2.1)] |
102509 | M | 214948![]() |
- | Irish Traveller | Global developmental delay | Immunodeficiency 54 | PMID:16532402 [Fam.A:IV.12(P3)]; PMID:22354167 [Fam.A:IV.12(P1.3)] |
102511 | M | 214948![]() |
- | Irish Traveller | Global developmental delay | Immunodeficiency 54 | PMID:16532402 [Fam.A:IV.14(P4)]; PMID:22354167 [Fam.A:IV.14(P1.4)] |
102512 | F | 214948![]() |
- | Irish Traveller | Global developmental delay | Immunodeficiency 54 | PMID:16532402 [Fam.A:IV.15]; PMID:22354167 [Fam.A:IV.15(P1.5)] |
102677 | M | 214980![]() |
3 | Pakistani | Global developmental delay | JAK1 deficiency | PMID:28008925 [Patient(II.4)] |
102739 | F | 214984![]() |
- | Japanese | Moderate global developmental delay | Autoinflammation, immune dysregulation, and eosinophilia | PMID:35046931 [Patient(II.1)] |
103076 | F | 215099![]() |
- | Omani | Global developmental delay | Seizures, cortical blindness, microcephaly syndrome | PMID:33662367 [Fam.F5:V.5(P6)] |
103132 | M | 215102![]() |
- | Emirati | Global developmental delay | Seizures, cortical blindness, microcephaly syndrome | PMID:26463574 [Fam.MC36500:IV.6(IV.3)] |
103152 | F | 215104![]() |
0 | Omani | Global developmental delay | Seizures, cortical blindness, microcephaly syndrome | PMID:26463574 [Fam.MC2500:IV.9(MC2501)] |
103170 | F | 215104![]() |
0 | Omani | Global developmental delay | PMID:26463574 [Fam.MC2500:IV.10] | |
103171 | M | 215104![]() |
2 | Omani | Global developmental delay | Seizures, cortical blindness, microcephaly syndrome | PMID:26463574 [Fam.MC2500:IV.11] |
104005 | F | 215326![]() |
- | Global developmental delay | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:25359994 [Fam.1:II.1(P9)]; PMID:35677041 [Pt4] | |
104402 | M | 215523![]() |
2 | Turkish | Neurodevelopmental delay | Immunodeficiency 114 | PMID:36517554 [Fam.Pt1:IV.4(Pt2)] |
104414 | M | 215526![]() |
8 | Turkish | Mild global developmental delay | Early-onset atopic inflammation | PMID:36758835 [Patient(V.3)] |
104554 | M | 215551![]() |
- | Pakistani | Mild global developmental delay | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:27523608 [Fam.1:V.2(V:2)]; PMID:27559085 [Fam.1:V.2(P1)]; PMID:35587511 [Fam.G:II.2(4)]; PMID:34797715 [P1]; PMID:38914362 [Fam.A:V.2(023)] |
104570 | F | 215551![]() |
- | Pakistani | Global developmental delay | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:27523608 [Fam.1:IV.4(IV:4)]; PMID:27559085 [Fam.1:IV.3(NA)]; PMID:38914362 [Fam.A:V.7(028)] |
104580 | F | 215553![]() |
- | Turkish | Global developmental delay | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:27559085 [Fam.3:II.1(P3)]; PMID:35587511 [Fam.H:II.1(3)]; PMID:34797715 [P3]; PMID:38914362 [Fam.C:II.1(039)] |
104625 | M | 215559![]() |
- | Global developmental delay | X-linked multisystem autoinflammatory disease with immune dysregulation | PMID:37342957 [Fam.B:II.2(P2)] | |
104678 | F | 215569![]() |
- | Iranian | Neurodevelopmental delay | Severe early onset systemic inflammation and autoimmunity | PMID:37349293 [Fam.2:II.2(P2)] |
105261 | F | 215680 | - | Egyptian | Neurodevelopmental delay | Otofaciocervical syndrome 2 | PMID:37924468 [Patient(III.1)] |
105797 | M | 215879 | - | Global developmental delay | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:33864888 [S041] | |
106084 | F | 215940 | - | Global developmental delay | 4q24 deletion syndrome | PMID:150198 [Fam.EN:591]; PMID:35784294 [303816] | |
106086 | M | 215942 | - | Global developmental delay | 4q24 deletion syndrome | PMID:150198 [Fam.EP:593]; PMID:35784294 [384471] | |
106246 | F | 215977 | - | Caucasian | Global developmental delay | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.UU:III.11(UU.III.7 (111))]; PMID:29305966 [Fam.IV.2:III.2(III.2)] |
106248 | F | 215977 | - | Caucasian | Global developmental delay | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.UU:III.15(UU.III.10 (113))]; PMID:29305966 [Fam.IV.2:III.4(III.5)] |
106250 | M | 215977 | - | Caucasian | Global developmental delay | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.UU:III.5(UU.III.4 (109))]; PMID:29305966 [Fam.IV.2:III.6(III.8)] |
106281 | M | 215977 | - | Caucasian | Global developmental delay | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.UU:V.1(UU.V.1 (121))]; PMID:29305966 [Fam.IV.2:V.3(V.3)] |
106448 | F | 216016![]() |
- | Japanese | Neurodevelopmental delay | Autoinflammation, panniculitis, and dermatosis syndrome 2 | PMID:38914362 [Fam.R:II.1(130)]; PMID:38652464 [Fam.1:II.1(Patient)] |
106654 | M | 216101![]() |
0 | Syrian | Global developmental delay | Intellectual disability due to EZR deficiency | PMID:25504542 [Fam.MR037:IV.1(IV-1)] |
106667 | M | 216101![]() |
0 | Syrian | Global developmental delay | Intellectual disability due to EZR deficiency | PMID:25504542 [Fam.MR037:IV.3(IV-3)] |
107161 | F | 216366![]() |
- | Sri Lankan Tamil | Global developmental delay | Adenosine deaminase 2 deficiency | PMID:26607704 [P1(II.1)] |
107212 | F | 216374 | 1,- | Arab | Global developmental delay,Neurodevelopmental delay | Combined immunodeficiency 37 | PMID:31775018 [Patient] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).