OBO ID: DOID:0070012
Term Name: Seckel syndrome 5 Search Ontology:
Synonyms:
  • SCKL5
Definition: A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/21131973
References:
Ontology: Human Disease   ( DOID:0070012 )
OTHER Seckel syndrome 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CEP152 Seckel syndrome 5 613823
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None