Ataxia-oculomotor apraxia type 1

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Name:
Ataxia-oculomotor apraxia type 1
Description:
A rare autosomal recessive cerebellar ataxia, characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.
ORPHAcode:
1168
Synonyms:
AOA1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14