OBO ID: DOID:0081169
Term Name: Leber congenital amaurosis 19 Search Ontology:
Synonyms:
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the USP45 gene on chromosome 6q16. https://pubmed.ncbi.nlm.nih.gov/3057356/
References:
Ontology: Human Disease   ( DOID:0081169 )
Relationships
is a type of:
OTHER Leber congenital amaurosis 19 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
USP45 ?Leber congenital amaurosis 19 618513
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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