OBO ID: DOID:0080232 |
Term Name: | autosomal dominant intellectual developmental disorder 51 | Search Ontology: | |
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Definition: | An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KMT5B gene on chromosome 11q13. https://pubmed.ncbi.nlm.nih.gov/28191889/ | ||
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Ontology: | Human Disease ( DOID:0080232 ) |
OTHER autosomal dominant intellectual developmental disorder 51 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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