OBO ID: DOID:0110716 |
Term Name: | Warburg micro syndrome 1 | Search Ontology: | |
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Definition: | A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21. https://www.ncbi.nlm.nih.gov/pubmed/20512159 | ||
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Ontology: | Human Disease ( DOID:0110716 ) |
OTHER Warburg micro syndrome 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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