ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Spinocerebellar ataxia with axonal neuropathy type 2

Amyotrophic lateral sclerosis type 4

PIK3R5	(UniProt - OMIM)		SETX	(UniProt - OMIM)
SETX	(UniProt - OMIM)

Citations in the biomedical literature:

Spinocerebellar ataxia with axonal neuropathy type 2		Amyotrophic lateral sclerosis type 4
	Synonym(s): - AOA2 - Ataxia - oculomotor apraxia type 2 - SCAN 2 - SCAR1		Synonym(s): - ALS4 - Distal hereditary motor neuropathy with upper motor neuron signs - dHMN with upper motor neuron signs

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - 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: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.