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Human Disease
autosomal dominant intellectual developmental disorder 47
- Term ID
- DOID:0080238
- Synonyms
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- autosomal dominant mental retardation 47
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the STAG1 gene on chromosome 3q22. https://pubmed.ncbi.nlm.nih.gov/28119487/
- References
- Ontology
- Human Disease ( DOID:0080238 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models