OBO ID: DOID:0070007
Term Name: Seckel syndrome 1 Search Ontology:
Synonyms:
  • microcephalic primordial dwarfism I
  • SCKL1
Definition: A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23. https://www.ncbi.nlm.nih.gov/pubmed/12640452
References:
Ontology: Human Disease   ( DOID:0070007 )
OTHER Seckel syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATR Seckel syndrome 1 210600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None