spastic ataxia 4
human disease
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spastic ataxia 4
Summary
spastic ataxia 4 is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- spastic ataxia 4's instance of is recorded as developmental defect during embryogenesis[3].
- spastic ataxia 4's instance of is recorded as rare disease[4].
- spastic ataxia 4's instance of is recorded as class of disease[5].
- spastic ataxia 4 is a type of spastic ataxia[6].
- spastic ataxia 4 is a type of autosomal recessive spastic ataxia[7].
- spastic ataxia 4 is a type of metabolic disease with dementia[8].
- spastic ataxia 4 is a type of combined oxidative phosphorylation deficiency[9].
- spastic ataxia 4 is a type of autosomal recessive disease[10].
- spastic ataxia 4's genetic association is recorded as MTPAP[11].
- spastic ataxia 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050943[12].
- spastic ataxia 4's exact match is recorded as http://identifiers.org/doid/DOID:0050943[13].
- spastic ataxia 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_254343[14].
- spastic ataxia 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
spastic ataxia 4 is known by 7 alternative names across languages and contexts.[2]