Search Ontology:
Human Disease

Vissers-Bodmer syndrome

Term ID
DOID:0081397
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models