Search Ontology:
Human Disease

chromosome 14q11-q22 deletion syndrome

Term ID
DOID:0060392
Synonyms
  • 14q11.2 microdeletion syndrome
Definition
A chromosomal deletion syndrome that is characterized by microcephaly, dysmorphic facies, psychomotor delay and failure to thrive, has_material_basis_in isolated cases of partial deletion of the long arm of chromosome 14. https://pubmed.ncbi.nlm.nih.gov/21744488
References
Ontology
Human Disease   ( DOID:0060392 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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