Delayed fine motor development

Symptom Information:

Symptom ID: HPO:0010862
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Motor delay
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 fine motor development(HPO:0010862)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)