OBO ID: DOID:0070006
Term Name: Seckel syndrome 6 Search Ontology:
Synonyms:
  • SCKL6
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22. https://www.ncbi.nlm.nih.gov/pubmed/21983783
References:
Ontology: Human Disease   ( DOID:0070006 )
Relationships
is a type of:
OTHER Seckel syndrome 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CEP63 ?Seckel syndrome 6 614728
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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