OBO ID: DOID:0111150
Term Name: autosomal dominant isolated ectopia lentis 1 Search Ontology:
Synonyms:
  • ECTOL1
Definition: An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/15054843
References:
Ontology: Human Disease   ( DOID:0111150 )
Relationships
is a type of:
OTHER autosomal dominant isolated ectopia lentis 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FBN1 Ectopia lentis, familial 129600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.