familial encephalopathy with neuroserpin inclusion bodies

Summary

familial encephalopathy with neuroserpin inclusion bodies is a rare disease^[1]. It draws 18 Wikipedia views per month (rare_disease category, ranking #236 of 627).^[2]

Key Facts

• familial encephalopathy with neuroserpin inclusion bodies's instance of is recorded as rare disease^[3].
• familial encephalopathy with neuroserpin inclusion bodies's instance of is recorded as class of disease^[4].
• familial encephalopathy with neuroserpin inclusion bodies is a type of neurodegeneration^[5].
• familial encephalopathy with neuroserpin inclusion bodies is a type of nervous system heredodegenerative disease^[6].
• familial encephalopathy with neuroserpin inclusion bodies is a type of genetic disease^[7].
• familial encephalopathy with neuroserpin inclusion bodies is a type of autosomal dominant disease^[8].
• familial encephalopathy with neuroserpin inclusion bodies's ICD-9-CM is recorded as 348.39^[9].
• familial encephalopathy with neuroserpin inclusion bodies's health specialty is recorded as neurology^[10].
• familial encephalopathy with neuroserpin inclusion bodies's genetic association is recorded as SERPINI1^[11].
• familial encephalopathy with neuroserpin inclusion bodies's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050831^[12].
• familial encephalopathy with neuroserpin inclusion bodies's exact match is recorded as http://identifiers.org/doid/DOID:0050831^[13].
• familial encephalopathy with neuroserpin inclusion bodies's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85110^[14].
• familial encephalopathy with neuroserpin inclusion bodies's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].

Why It Matters

familial encephalopathy with neuroserpin inclusion bodies draws 18 Wikipedia views per month (rare_disease category, ranking #236 of 627).^[2]