OBO ID: DOID:0110261
Term Name: cataract 35 Search Ontology:
Synonyms:
  • autosomal recessive congenital nuclear cataract 1
  • cataract 35, congenital nuclear
  • CATCN1
  • CTRCT35
Definition: A cataract that has_material_basis_in variation in the region 19q13. https://www.ncbi.nlm.nih.gov/pubmed/15671291
References:
Ontology: Human Disease   ( DOID:0110261 )
Relationships
is a type of:
OTHER cataract 35 PAGES
GENES INVOLVED No data available
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.