Neuroaxonal dystrophy

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Neuroaxonal dystrophy (in some patients) [OMIM:Neuroaxonal dystrophy (in some patients)]
Quality:
Cross references:
OMIM: "Neuroaxonal dystrophy" [OMIM:Neuroaxonal dystrophy]
OMIM: "Neuroaxonal dystrophy (in some patients)" [OMIM:Neuroaxonal dystrophy (in some patients)]
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)