MeSH Browser

MeSH Supplementary: Furukawa Takagi Nakao syndrome
Unique ID: C538193
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538193
Registry Numbers: 0
Heading Mapped to: *Cerebellar Ataxia; *Diabetes Mellitus; *Muscular Atrophy; *Retinitis Pigmentosa
Frequency: 0
Note: Hereditary muscular atrophy with ataxia, retinitis pigmentosa, and diabetes mellitus
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Furukawa Takagi Nakao syndrome MeSH Supplementary Concept Data 2025