OBO ID: DOID:0060390
Term Name: distal 10q deletion syndrome Search Ontology:
Synonyms:
  • chromosome 10q26 deletion syndrome
  • distal monosomy 10q
  • monosomy 10qter
  • telomeric deletion 10q
  • terminal chromosome 10q26 deletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10. https://rarediseases.info.nih.gov/diseases/3711/chromosome-10q-deletion
References:
Ontology: Human Disease   ( DOID:0060390 )
Relationships
is a type of:
OTHER distal 10q deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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