Axonal degeneration

Symptom Information:

Symptom ID: HPO:0040078
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 10 / 7739
Resource: HPO

All diseases associated with this symptom:

Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Amyotrophic lateral sclerosis type 4 (Orphanet:357043)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (Orphanet:100044)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S (OMIM:616155)
CREST syndrome (Orphanet:90290)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA (OMIM:608720)
Neuralgic amyotrophy (Orphanet:2901)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)