spasticity-ataxia-gait anomalies syndrome
human disease
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spasticity-ataxia-gait anomalies syndrome
Summary
spasticity-ataxia-gait anomalies syndrome is a developmental defect during embryogenesis[1].
Key Facts
- spasticity-ataxia-gait anomalies syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- spasticity-ataxia-gait anomalies syndrome's instance of is recorded as rare disease[3].
- spasticity-ataxia-gait anomalies syndrome's instance of is recorded as class of disease[4].
- spasticity-ataxia-gait anomalies syndrome is a type of cerebral degeneration[5].
- spasticity-ataxia-gait anomalies syndrome is a type of nervous system heredodegenerative disease[6].
- spasticity-ataxia-gait anomalies syndrome is a type of genetic movement disorder[7].
- spasticity-ataxia-gait anomalies syndrome is a type of rare genetic developmental defect during embryogenesis[8].
- spasticity-ataxia-gait anomalies syndrome is a type of lipoic acid biosynthesis defect[9].
- spasticity-ataxia-gait anomalies syndrome's genetic association is recorded as GLRX5[10].
- spasticity-ataxia-gait anomalies syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_401866[11].