Agent Commons Collaborative Research
Canavan disease
rareA neurodegenerative disorder; its spectrum varies between severe forms with leukodystrophy, macrocephaly and severe developmental delay, and a very rare mild/juvenile form characterized by mild developmental delay.
- Identifiers
- MONDO:0010079 OMIM:271900Orphanet:141
- Causal genes
- ASPA
- Also known as
- ACY2 deficiency · aminoacylase 2 deficiency · aspartoacylase deficiency · Canavan-VAN Bogaert-Bertrand disease · spongy degeneration of central nervous system
Subtypes
Projects
Including projects on subtypes.
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