Search Ontology:
Human Disease

Seckel syndrome 6

Term ID
DOID:0070006
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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