OBO ID: DOID:0070122 |
Term Name: | Meckel syndrome 8 | Search Ontology: | |
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Definition: | A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TCTN2 gene on chromosome 12q24.31. https://www.ncbi.nlm.nih.gov/pubmed/21462283 | ||
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Ontology: | Human Disease ( DOID:0070122 ) |
OTHER Meckel syndrome 8 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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