Search Ontology:
Human Disease
Vissers-Bodmer syndrome
- Term ID
- DOID:0081397
- Synonyms
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- Definition
- A syndrome that is characterized by global developmental delay with variably impaired intellectual development, speech delay, motor delay, and behavioral abnormalities apparent from infancy and that has_material_basis_in heterozygous mutation in the CNOT1 gene on chromosome 16q21. https://pubmed.ncbi.nlm.nih.gov/32553196/
- References
- Ontology
- Human Disease ( DOID:0081397 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models