ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Early-onset spastic ataxia-neuropathy syndrome

Spinocerebellar ataxia type 28

Citations in the biomedical literature:

Early-onset spastic ataxia-neuropathy syndrome		Spinocerebellar ataxia type 28
	Synonym(s): - AFG3L2-associated spastic ataxia-neuropathy syndrome - Autosomal recessive spastic ataxia type 5 - SPAX5		Synonym(s): - SCA28

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		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		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537205

No signs/symptoms info available.