Delayed gross motor development

Symptom Information:

Symptom ID: HPO:0002194
Synonyms:
Delayed gross motor skills [HPO:0002194]
Delayed motor skills [HPO:0002194]
Developmental delay, gross motor [HPO:0002194]
Gross motor delay [HPO:0002194]
Limited gross motor development [HPO:0002194]
Delayed gross motor development [OMIM:Delayed gross motor development]
Delayed motor skills [OMIM:Delayed motor skills]
Developmental delay, gross motor [OMIM:Developmental delay, gross motor]
Gross motor delay [OMIM:Gross motor delay]
Limited gross motor development [OMIM:Limited gross motor development]
Delayed gross motor development (in some patients) [OMIM:Delayed gross motor development (in some patients)]
Gross motor delay (in one family) [OMIM:Gross motor delay (in one family)]
Gross motor developmental delay [OMIM:Gross motor developmental delay]
Gross motor skill delay (infancy) [OMIM:Gross motor skill delay (infancy)]
Gross motor delay [MedDRA:10069118]
Quality:
Cross references:
OMIM: "Delayed gross motor development" [OMIM:Delayed gross motor development]
OMIM: "Delayed motor skills" [OMIM:Delayed motor skills]
OMIM: "Developmental delay, gross motor" [OMIM:Developmental delay, gross motor]
OMIM: "Gross motor delay" [OMIM:Gross motor delay]
OMIM: "Limited gross motor development" [OMIM:Limited gross motor development]
OMIM: "Delayed gross motor development (in some patients)" [OMIM:Delayed gross motor development (in some patients)]
OMIM: "Gross motor delay (in one family)" [OMIM:Gross motor delay (in one family)]
OMIM: "Gross motor developmental delay" [OMIM:Gross motor developmental delay]
OMIM: "Gross motor skill delay (infancy)" [OMIM:Gross motor skill delay (infancy)]
Is a (Direct Parents):
HPO         Motor delay
MedDRA Developmental motor skills disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Cognitive impairment(HPO:0100543)
                   Global developmental delay(HPO:0001263)
                      Motor delay(HPO:0001270)
                         Delayed gross motor development(HPO:0002194)
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3C syndrome (Orphanet:7)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Bosley-Salih-Alorainy syndrome (Orphanet:69737)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Childhood-onset hypophosphatasia (Orphanet:247667)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Cortical dysplasia - focal epilepsy syndrome (Orphanet:163681)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Galactose epimerase deficiency (Orphanet:79238)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Infantile dystonia-parkinsonism (Orphanet:238455)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Joubert syndrome with renal defect (Orphanet:220497)
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES (OMIM:613670)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MENTAL RETARDATION, X-LINKED 9 (OMIM:309549)
MERRF (Orphanet:551)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
NEMALINE MYOPATHY 5 (OMIM:605355)
NEMALINE MYOPATHY 7 (OMIM:610687)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
USHER SYNDROME, TYPE IIIB (OMIM:614504)