Search Ontology:
Human Disease

Leber congenital amaurosis 7

Term ID
DOID:0110333
Synonyms
  • LCA7
Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9537410
References
Ontology
Human Disease   ( DOID:0110333 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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