Search Ontology:
Human Disease

GM1 gangliosidosis type 2

Term ID
DOID:0080501
Synonyms
  • juvenile GM1 gangliosidosis
Definition
A GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age. https://www.ncbi.nlm.nih.gov/pubmed/12644936
References
Ontology
Human Disease   ( DOID:0080501 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.