Generalized dystonia
Symptom Information:
Symptom ID: | HPO:0007325 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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 movement(HPO:0100022) Dystonia(HPO:0001332) Generalized dystonia(HPO:0007325) MedDRA: |
||
Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Developmental malformations - deafness - dystonia | (Orphanet:79107) |
Isolated sulfite oxidase deficiency | (Orphanet:99731) |
Lesch-Nyhan syndrome | (Orphanet:510) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Primary dystonia, DYT4 type | (Orphanet:98805) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |