CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 616280
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001284) Areflexia 198 / 7739
2
(HPO:0003477) Peripheral axonal neuropathy 62 / 7739
3
(HPO:0002936) Distal sensory impairment 96 / 7739
4
(HPO:0003376) Steppage gait 41 / 7739
5
(HPO:0009027) Foot dorsiflexor weakness 45 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: