Delayed gross motor development
Basic details
Preferred term: Delayed gross motor development
Alt. terms: Delayed gross motor skills | Delayed motor skills | Developmental delay, gross motor | Gross motor delay | Limited gross motor development
HPO term: Delayed gross motor development
HPO code: HP:0002194
GenIA ID: 2323
Last updated on: 2021-08-02 21:50:33
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -
Description
A type of motor delay characterized by a delay in acquiring the ability to control the large muscles of the body for walking, running, sitting, and crawling.
Hierarchical classification
PARENT terms
TERM
Delayed gross motor development
Reported patients added to GenIA DB
| SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
|---|---|---|---|---|---|---|---|
| 102417 | F | 214946 |
0 | Dutch | Motor delay | Stuve-Wiedemann syndrome 2 | PMID:31914175 [Fam.C:II.3] |
| 103051 | M | 215095 |
0 | Finnish | Motor delay | Seizures, cortical blindness, microcephaly syndrome | PMID:33662367 [Fam.F1:II.7(P1)] |
| 103110 | M | 215099 |
- | Omani | Delayed gross motor development | Seizures, cortical blindness, microcephaly syndrome | PMID:33662367 [Fam.F5:V.2(P7)] |
| 103116 | F | 215101 |
- | Saudi | Motor delay | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [P1(IV.4)] |
| 103128 | F | 215101 |
- | Saudi | Motor delay | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.5] |
| 103129 | F | 215101 |
- | Saudi | Motor delay | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.6] |
| 106085 | F | 215941 | - | Delayed gross motor development | 4q24 deletion syndrome | PMID:150198 [Fam.EO:592]; PMID:35784294 [314461] | |
| 106847 | M | 216169 |
4 | Caucasian | Motor delay | Adenosine deaminase 2 deficiency | PMID:29963054 [P1(II.1)] |
| 107212 | F | 216374 | 5 | Arab | Delayed ability to walk with support | 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).