Dysgraphia

Symptom Information:

Symptom ID: HPO:0010526
Synonyms:
Dysgraphia (finding) [Orphanet:43500]
Agraphia (finding) [Orphanet:43500]
Dysgraphia [Orphanet:43500]
Agraphia [Orphanet:43500]
Dysgraphia [OMIM:Dysgraphia]
Alexia/agraphia/writing/reading troubles [Orphanet:43500]
Agraphia [MedDRA:10001508]
Dysgraphia [MedDRA:10058319]
Developmental writing disorder [MedDRA:10058319]
Disorder of written expression [MedDRA:10058319]
Writing impaired [MedDRA:10058319]
Dystaxic writing [MedDRA:10058319]
Quality:
Cross references:
Orphanet:43500 "Alexia/agraphia/writing/reading troubles" [Orphanet:43500]
OMIM: "Dysgraphia" [OMIM:Dysgraphia]
UMLS:C0234144 "Dysgraphia" [HPO:0010526]
UMLS:C0234144 "Dysgraphia" [Orphanet:43500]
UMLS:C0001825 "Agraphia" [Orphanet:43500]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Specific cognitive ability disturbances
HPO         Neurological speech impairment
MedDRA Cortical dysfunction NEC
Orphanet Alexia
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)
                Neurological speech impairment(HPO:0002167)
                   Dysgraphia(HPO:0010526)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Cortical dysfunction NEC(MedDRA:10011168)
          Dysgraphia(HPO:0010526)
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Marden-Walker syndrome (Orphanet:2461)
Pyruvate carboxylase deficiency (Orphanet:3008)
Spinocerebellar ataxia type 21 (Orphanet:98773)