MeSH Browser

MeSH Supplementary: Hyperexplexia hereditary
Unique ID: C538136
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538136
Entry Term(s): Congenital stiff person syndrome; Exagerrated startle reflex; Familial startle disease; Kok disease; Stiff baby syndrome
Registry Numbers: 0
Heading Mapped to: *Muscle Rigidity
Frequency: 10
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Concept UI: M0532597
Registry Numbers: 0
Terms: Hyperexplexia hereditary Preferred Term
Term UI T744837
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Familial startle disease
Term UI T744840
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Kok disease
Term UI T744839
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Stiff baby syndrome
Term UI T744838
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Congenital stiff person syndrome
Term UI T744842
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Exagerrated startle reflex
Term UI T744841
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Hyperexplexia hereditary MeSH Supplementary Concept Data 2025