Search Ontology:
Human Disease

chromosome 1q21.1 deletion syndrome

Term ID
DOID:0060411
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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