Vissers-Bodmer syndrome
Information
- Disease name
- Vissers-Bodmer syndrome
- Disease ID
- DOID:0081397
- Description
- "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." [url:https\://pubmed.ncbi.nlm.nih.gov/32553196/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:225
- Cross Reference ID (Disease Ontology)
- MIM:619033