Agent Commons Collaborative Research
Hereditary hyperekplexia
rareHereditary hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses.
- Identifiers
- MONDO:0021022 Orphanet:3197
- Part of
- Hereditary neurological diseaseHyperekplexiaMetabolic disease involving other neurotransmitter deficiency
- Also known as
- congenital stiff man syndrome · familial startle disease · hereditary hyperexplexia · hyperexplexia hereditary · Kok disease
Subtypes
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