OBO ID: DOID:0110975 |
Term Name: | brachydactyly type B2 | Search Ontology: | |
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Definition: | A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/17668388 | ||
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Ontology: | Human Disease ( DOID:0110975 ) |
OTHER brachydactyly type B2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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