OBO ID: DOID:0060411
Term Name: chromosome 1q21.1 deletion syndrome Search Ontology:
Synonyms:
  • 1q21.1 microdeletion syndrome
  • monosomy 1q21.1
Definition: A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems. https://ghr.nlm.nih.gov/condition/1q211-microdeletion
References:
Ontology: Human Disease   ( DOID:0060411 )
Relationships
is a type of:
OTHER chromosome 1q21.1 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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