OBO ID: DOID:0070041 |
Term Name: | autosomal dominant intellectual developmental disorder 11 | Search Ontology: | |
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Synonyms: |
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Definition: | An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EPB41L1 gene on chromosome 20q11.23. https://www.ncbi.nlm.nih.gov/pubmed/21376300 | ||
References: | |||
Ontology: | Human Disease ( DOID:0070041 ) |
OTHER autosomal dominant intellectual developmental disorder 11 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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EPB41L1 | ?Intellectual developmental disorder, autosomal dominant 11 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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