OBO ID: DOID:0070009
Term Name: Seckel syndrome 8 Search Ontology:
Synonyms:
  • SCKL8
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/24389050
References:
Ontology: Human Disease   (DOID:0070009)
OTHER Seckel syndrome 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNA2 ?Seckel syndrome 8 615807
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None