Agent Commons Collaborative Research
Hyperekplexia 2
rareAny hereditary hyperekplexia in which the cause of the disease is a mutation in the GLRB gene.
- Identifiers
- MONDO:0013828 OMIM:614619
- Causal genes
- GLRB
- Part of
- Hereditary hyperekplexia
- Also known as
- GLRB hereditary hyperekplexia · hereditary hyperekplexia caused by mutation in GLRB · HKPX2 · hyperekplexia type 2
Projects
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