MeSH Browser

MeSH Supplementary: Segawa syndrome, autosomal recessive
Unique ID: C537537
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537537
Entry Term(s): Autosomal Recessive Infantile Parkinsonism; DOPA responsive dystonia, autosomal recessive; Dopa-Responsive Dystonia, Autosomal Recessive; Dystonia, DOPA responsive, autosomal recessive; Dystonia, Dopa-Responsive, Autosomal Recessive; Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia, Autosomal Recessive; Parkinsonism, infantile, autosomal recessive; Th-Deficient Drd; Tyrosine Hydroxylase Deficiency
Registry Numbers: 0
Heading Mapped to: Dystonic Disorders / congenital
Frequency: 28
Date of Entry: 2010/08/25
Revision Date: 2023/05/31

Segawa syndrome, autosomal recessive MeSH Supplementary Concept Data 2024