autosomal recessive ataxia, Beauce type
gene mutations
Press Enter · cited answer in seconds
0 sources
autosomal recessive ataxia, Beauce type
Summary
autosomal recessive ataxia, Beauce type is a developmental defect during embryogenesis[1].
Key Facts
- autosomal recessive ataxia, Beauce type's instance of is recorded as developmental defect during embryogenesis[2].
- autosomal recessive ataxia, Beauce type's instance of is recorded as rare disease[3].
- autosomal recessive ataxia, Beauce type's instance of is recorded as class of disease[4].
- autosomal recessive ataxia, Beauce type is a type of autosomal recessive cerebellar ataxia[5].
- autosomal recessive ataxia, Beauce type's health specialty is recorded as neurology[6].
- autosomal recessive ataxia, Beauce type's genetic association is recorded as SYNE1[7].
- autosomal recessive ataxia, Beauce type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_88644[8].