Mondo Disease Ontology
29 terms(s) returned
| Term Type: | Record: 1 to 29 of 29 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- Charlevoix-Saguenay spastic ataxia
- Lichtenstein-Knorr syndrome
- RIDDLE syndrome
- ataxia with oculomotor apraxia type 3
- autosomal recessive ataxia due to ubiquinone deficiency
- autosomal recessive ataxia, Beauce type
- autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
- autosomal recessive congenital cerebellar ataxia
- autosomal recessive degenerative and progressive cerebellar ataxia
- autosomal recessive metabolic cerebellar ataxia
- autosomal recessive spinocerebellar ataxia 10
- autosomal recessive spinocerebellar ataxia 14
- autosomal recessive spinocerebellar ataxia 16
- autosomal recessive spinocerebellar ataxia 20
- autosomal recessive spinocerebellar ataxia 7
- autosomal recessive syndromic cerebellar ataxia
- infantile-onset autosomal recessive nonprogressive cerebellar ataxia
- spinocerebellar ataxia, autosomal recessive 22
- spinocerebellar ataxia, autosomal recessive 24
- spinocerebellar ataxia, autosomal recessive 25
- spinocerebellar ataxia, autosomal recessive 26
- spinocerebellar ataxia, autosomal recessive 27
- spinocerebellar ataxia, autosomal recessive 28
- spinocerebellar ataxia, autosomal recessive 29
- spinocerebellar ataxia, autosomal recessive 30
- spinocerebellar ataxia, autosomal recessive 31
- spinocerebellar ataxia, autosomal recessive 32
- spinocerebellar ataxia, autosomal recessive 33
- spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
