autosomal recessive ataxia, Beauce type

Summary

autosomal recessive ataxia, Beauce type is a developmental defect during embryogenesis^[1]. It draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]

Key Facts

• autosomal recessive ataxia, Beauce type's instance of is recorded as developmental defect during embryogenesis^[3].
• autosomal recessive ataxia, Beauce type's instance of is recorded as rare disease^[4].
• autosomal recessive ataxia, Beauce type's instance of is recorded as class of disease^[5].
• autosomal recessive ataxia, Beauce type's subclass of is recorded as autosomal recessive cerebellar ataxia^[6].
• autosomal recessive ataxia, Beauce type's OMIM ID is recorded as 610743^[7].
• autosomal recessive ataxia, Beauce type's Orphanet ID is recorded as 88644^[8].
• autosomal recessive ataxia, Beauce type's health specialty is recorded as neurology^[9].
• autosomal recessive ataxia, Beauce type's genetic association is recorded as SYNE1^[10].
• autosomal recessive ataxia, Beauce type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_88644^[11].
• autosomal recessive ataxia, Beauce type's UMLS CUI is recorded as C3683483^[12].
• autosomal recessive ataxia, Beauce type's UMLS CUI is recorded as C1853116^[13].
• autosomal recessive ataxia, Beauce type's ICD-10-CM is recorded as G11.2^[14].
• autosomal recessive ataxia, Beauce type's GARD rare disease ID is recorded as 12234^[15].
• autosomal recessive ataxia, Beauce type's Mondo ID is recorded as MONDO_0012549^[16].
• autosomal recessive ataxia, Beauce type's SNOMED CT ID is recorded as 725433003^[17].
• autosomal recessive ataxia, Beauce type's Genetics Home Reference Conditions ID is recorded as autosomal-recessive-cerebellar-ataxia-type-1^[18].

Why It Matters

autosomal recessive ataxia, Beauce type draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]