MeSH Browser

MeSH Supplementary: Spastic paraplegia 11, autosomal recessive
Unique ID: C537483
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537483
Entry Term(s): Autosomal Recessive Spastic Paraplegia Complicated with Thin Corpus Callosum; Autosomal Recessive Spastic Paraplegia with Mental Impairment and Thin Corpus Callosum; Hsp-Tcc; Spastic Paraplegia Type 11; Spastic Paraplegia, Autosomal Recessive, Complicated, with Thin Corpus Callosum; Spastic Paraplegia, Autosomal Recessive, with Mental Impairment and Thin Corpus Callosum; Spg11-Related Hereditary Spastic Paraplegia with Thin Corpus Callosum
Registry Numbers: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 37
Note: Autosomal recessive hereditary spastic paraplegia, complicated with a thin corpus callosum
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Spastic paraplegia 11, autosomal recessive MeSH Supplementary Concept Data 2025