8A03.1Y Other specified hereditary ataxia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Other specified hereditary ataxia
Autosomal recessive ataxia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Ataxia due to Marinesco-Sjögren syndrome
Autosomal recessive ataxias due to POLG mutations
Ataxia due to POLG mutations MIRAS
Autosomal recessive ataxias due to POLG mutations SANDO
Other autosomal recessive ataxia
Harding ataxia
Early onset cerebellar ataxia with retained tendon reflex
X-linked ataxia
X-linked intellectual deficit - ataxia - apraxia
X-linked intellectual deficit, South African type
X-linked intellectual deficit - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy
Christianson syndrome
X-linked spinocerebellar ataxia type 1
X-linked spinocerebellar ataxia type 3
X-linked spinocerebellar ataxia type 4
Fragile X–associated tremor or ataxia syndrome
Autosomal dominant ataxia
Autosomal dominant cerebellar ataxia
Autosomal dominant spastic ataxia
Dominant ataxia with unknown mutation
Progressive Ataxia palatal tremor syndrome-GFAP gene mutation

Thank you for choosing Find-A-Code, please Sign In to remove ads.