Search Ontology:
Human Disease

chromosome 2p12-p11.2 deletion syndrome

Term ID
DOID:0060414
Synonyms
Definition
A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 2p12-p11.2 region. https://pubmed.ncbi.nlm.nih.gov/19764038/
References
Ontology
Human Disease   ( DOID:0060414 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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