Axonal degeneration
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 7 / 7739 | |
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All diseases associated with this symptom:
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Autosomal dominant Charcot-Marie-Tooth disease type 2M | (Orphanet:228179) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B | (Orphanet:100044) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA | (OMIM:608720) |
Neuralgic amyotrophy | (Orphanet:2901) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |