MeSH Browser

MeSH Supplementary: Joubert Syndrome 10
Unique ID: C567582
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567582
Entry Term(s): JBTS10
Registry Numbers: 0
Heading Mapped to: *Cerebellar Diseases; *Muscle Hypotonia; *Genetic Diseases, X-Linked
Frequency: 5
Note: mutation in OFD1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Joubert Syndrome 10 MeSH Supplementary Concept Data 2024