Search Ontology:
Human Disease

hereditary congenital ptosis 2

Term ID
DOID:0061148
Synonyms
Definition
A hereditary congenital ptosis that has_material_basis_in linkage to the X chromosome. https://pubmed.ncbi.nlm.nih.gov/10739771/
References
Ontology
Human Disease   ( DOID:0061148 )
Relationships
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.