Search Ontology:
Human Disease

Seckel syndrome 9

Term ID
DOID:0070005
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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