OBO ID: DOID:0070005
Term Name: Seckel syndrome 9 Search Ontology:
Synonyms:
  • SCKL9
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/26595769
References:
Ontology: Human Disease   ( DOID:0070005 )
Relationships
is a type of:
OTHER Seckel syndrome 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TRAIP Seckel syndrome 9
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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