OBO ID: DOID:0110331
Term Name: Leber congenital amaurosis 3 Search Ontology:
Synonyms:
  • LCA3
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31. https://www.ncbi.nlm.nih.gov/pubmed/19268277
References:
Ontology: Human Disease   ( DOID:0110331 )
Relationships
is a type of:
OTHER Leber congenital amaurosis 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPATA7 Retinitis pigmentosa 94, variable age at onset, autosomal recessive 604232
Leber congenital amaurosis 3 604232
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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