Delayed gross motor development
Symptom Information:
Symptom ID: | HPO:0002194 | |||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |