spastic ataxia 2
human disease
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spastic ataxia 2
Summary
spastic ataxia 2 is a developmental defect during embryogenesis[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- spastic ataxia 2's instance of is recorded as developmental defect during embryogenesis[3].
- spastic ataxia 2's instance of is recorded as rare disease[4].
- spastic ataxia 2's instance of is recorded as class of disease[5].
- spastic ataxia 2 is a type of spastic ataxia[6].
- spastic ataxia 2 is a type of autosomal recessive spastic ataxia[7].
- spastic ataxia 2 is a type of autosomal recessive complex spastic paraplegia[8].
- spastic ataxia 2 is a type of autosomal recessive disease[9].
- spastic ataxia 2's NCI Thesaurus ID is recorded as C177252[10].
- spastic ataxia 2's genetic association is recorded as KIF1C[11].
- spastic ataxia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050941[12].
- spastic ataxia 2's exact match is recorded as http://identifiers.org/doid/DOID:0050941[13].
- spastic ataxia 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_397946[14].
- spastic ataxia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
spastic ataxia 2 is known by 8 alternative names across languages and contexts.[2]