OBO ID: DOID:0070010
Term Name: Seckel syndrome 4 Search Ontology:
Synonyms:
  • SCKL4
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the CENPJ gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/20522431
References:
Ontology: Human Disease   ( DOID:0070010 )
Relationships
is a type of:
OTHER Seckel syndrome 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CENPJ ?Seckel syndrome 4 613676
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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