Search Ontology:
Human Disease

chromosome 18p deletion syndrome

Term ID
DOID:0060406
Synonyms
  • 18p- syndrome
  • De Grouchy syndrome
  • monosomy 18p
Definition
A chromosomal deletion syndrome that has_material_basis_in partial or complete deletion of the short arm of chromosome 18. https://pubmed.ncbi.nlm.nih.gov/16691587
References
Ontology
Human Disease   ( DOID:0060406 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models