Mondo Disease Ontology
13 terms(s) returned
| Term Type: | Record: 1 to 13 of 13 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- 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
