Search Ontology:
Human Disease

chromosome 19q13.11 deletion syndrome

Term ID
DOID:0060408
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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