OBO ID: DOID:0070295 |
Term Name: | primary autosomal dominant microcephaly 18 | Search Ontology: | |
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Definition: | A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/27008544 | ||
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Ontology: | Human Disease ( DOID:0070295 ) |
OTHER primary autosomal dominant microcephaly 18 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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