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Autosomal recessive spastic paraplegia type 21
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Lethal ataxia with deafness and optic atrophy
Phosphoribosylpyrophosphate synthetase superactivity
X-linked Charcot-Marie-Tooth disease type 5
X-linked nonsyndromic sensorineural deafness type DFN
Synonym(s):
- Mast syndrome
- SPG21
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SPG21 Q9NZD8608181
No signs/symptoms info available.