OBO ID: DOID:0060408
Term Name: chromosome 19q13.11 deletion syndrome Search Ontology:
Synonyms:
  • 19q13.11 microdeletion syndrome
  • monosomy 19q13.11
Definition: A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties. https://pubmed.ncbi.nlm.nih.gov/24243649
References:
Ontology: Human Disease   ( DOID:0060408 )
OTHER chromosome 19q13.11 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None