MeSH Browser

MeSH Supplementary: Spastic paraplegia 9, autosomal dominant
Unique ID: C536868
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536868
Entry Term(s): Autosomal dominant spastic paraparesis; Bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy; Cataracts With Motor Neuronopathy, Short Stature, And Skeletal Abnormalities; Cataracts, motor neuronopathy, short stature and skeletal abnormalities; Spastic Paraparesis With Amyopathy, Cataracts, And Gastroesophageal Reflux
Registry Numbers: 0
Heading Mapped to: Bone and Bones / abnormalities; *Cataract; *Growth Disorders; *Spastic Paraplegia, Hereditary
Frequency: 4
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Spastic paraplegia 9, autosomal dominant MeSH Supplementary Concept Data 2025