OBO ID: DOID:0111723
Term Name: Jacobsen Syndrome Search Ontology:
Synonyms:
  • chromosome 11q deletion syndrome
  • Jacobsen distal 11q deletion syndrome
  • partial 11q monosomy syndrome
Definition: A chromosomal deletion syndrome that is characterized by growth retardation, psychomotor retardation, distinctive facial features, skeletal abnormalities, and isoimmune thrombocytopenia that has_material_basis_in deletion of terminal chromosome 11q. https://www.ncbi.nlm.nih.gov/pubmed/4134631
References:
Ontology: Human Disease   ( DOID:0111723 )
Relationships
is a type of:
OTHER Jacobsen Syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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