Search Ontology:
Human Disease

Cornelia de Lange syndrome 3

Term ID
DOID:0080507
Synonyms
  • CDLS3
  • Cornelia De Lange syndrome 3 with or without midline brain defects
Definition
A Cornelia de Lange syndrome that has_material_basis_in heterozygous mutation in the SMC3 gene on chromosome 10q25.2. https://www.ncbi.nlm.nih.gov/pubmed/25655089
References
Ontology
Human Disease   ( DOID:0080507 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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