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Giant axonal neuropathy
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
X-linked distal arthrogryposis multiplex congenita
Pseudohypoaldosteronism type 2E
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: D056768
Gene symbol UniProt reference OMIM reference
GAN Q9H2C0605379
No signs/symptoms info available.