Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 13
- Term ID
- DOID:0081098
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TRAPPC9 gene on chromosome 8q24. https://pubmed.ncbi.nlm.nih.gov/22549410/
- References
- Ontology
- Human Disease ( DOID:0081098 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models