OBO ID: DOID:0060392
Term Name: chromosome 14q11-q22 deletion syndrome Search Ontology:
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 chromosome 14q11-q22 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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