Neuroaxonal dystrophy
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
Is a (Whole tree): |
HPO:
MedDRA: |
||
Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT | (OMIM:608984) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-N-acetylgalactosaminidase deficiency type 3 | (Orphanet:79281) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |