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
  • GARD:8631
  • MESH:C538309
  • MIM:146390
  • NCI:C84521
  • ORDO:1598
  • SNOMEDCT_US_2023_03_01:205632001
  • UMLS_CUI:C0432442
Ontology
Human Disease   ( DOID:0060406 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations