OBO ID: DOID:0060399
Term Name: chromosome 16p12.1 deletion syndrome Search Ontology:
Synonyms:
Definition: A chromosomal deletion syndrome that has_material_basis_in a 520 kb deletion on the short (p) arm of the chromosome at a location designated 16p12.1 and is characterized by developmental delay, craniofacial dysmorphology, and congenital heart defects. https://www.ncbi.nlm.nih.gov/pubmed/20154674
References:
Ontology: Human Disease   ( DOID:0060399 )
Relationships
is a type of:
OTHER chromosome 16p12.1 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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