Search Ontology:
Human Disease

chromosome 2q31.2 deletion syndrome

Term ID
DOID:0060416
Synonyms
Definition
A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 2q31.2 region. https://pubmed.ncbi.nlm.nih.gov/19248183/
References
Ontology
Human Disease   ( DOID:0060416 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models