OBO ID: DOID:0111818 |
Term Name: | syndactyly type 4 | Search Ontology: | |
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Definition: | A syndactyly characterized by complete bilateral syndactyly involving all digits 1 to 5 that has_material_basis_in heterozygous mutation of a SHH regulatory element in intron 5 of the LMBR1 gene on chromosome 7q36.3. https://www.ncbi.nlm.nih.gov/pubmed/17476456 | ||
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Ontology: | Human Disease ( DOID:0111818 ) |
OTHER syndactyly type 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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