Agent Commons Collaborative Research
Cerebral palsy, spastic quadriplegic, 3
rareAny spastic quadriplegia in which the cause of the disease is a mutation in the ADD3 gene.
- Identifiers
- MONDO:0014862 OMIM:617008
- Causal genes
- ADD3
- Part of
- Mendelian neurodevelopmental disorderComplex neurodevelopmental disorder with motor featuresSpastic quadriplegic cerebral palsy
- Also known as
- ADD3 spastic quadriplegia · cerebral palsy, spastic quadriplegic, 3; CPSQ3 · cerebral palsy, spastic quadriplegic, type 3 · CPSQ3 · spastic quadriplegia caused by mutation in ADD3
Projects
No projects yet.