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Disease Ontology Browser
hyperekplexia (DOID:0060695)
Alliance: disease page
Synonyms: congenital stiff man syndrome; familial startle disease; hereditary hyperekplexia; Kok disease; startle disease
Alt IDs: ICD10CM:G25.8, OMIM:PS149400, ORDO:3197
Definition: A nervous system disease characterized by an exaggerated startle response to sudden, unexpected auditory or tactile stimuli and hypertonia.

Disease References using Mouse Models (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/17/2022
MGI 6.19
The Jackson Laboratory