OBO ID: DOID:0060673
Term Name: Peters anomaly Search Ontology:
Synonyms:
Definition: A corneal disease characterized by a central corneal leukoma and absence of the posterior corneal stroma and Descemet membrane that has_material_basis_in mutation in the PAX6 gene on chromosome 11p13, the PITX2 gene on chromosome 4q25, the CYP1B1 gene on chromosome 2p22.2, or the FOXC1 gene on chromosome 6p25.3. (3)
References:
Ontology: Human Disease   ( DOID:0060673 )
Relationships
is a type of:
OTHER Peters anomaly PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PAX6 Anterior segment dysgenesis 5, multiple subtypes 604229
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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.