Search Ontology:
Human Disease

Seckel syndrome 4

Term ID
DOID:0070010
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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