Axonal degeneration

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Axonal degeneration" [OMIM:Axonal degeneration]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 7 / 7739
Resource:

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)