Search Ontology:
Human Disease

congenital hypomyelinating neuropathy 2

Term ID
DOID:0070679
Synonyms
  • CHN2
Definition
A congenital hypomyelinating neuropathy that has_material_basis_in heterozygous mutation in the MPZ gene on chromosome 1q23. (2)
References
Ontology
Human Disease   ( DOID:0070679 )
Relationships
Other Pages
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.