Search Ontology:
Human Disease

Seckel syndrome 10

Term ID
DOID:0070008
Synonyms
  • SCKL10
Definition
A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/25105364
References
Ontology
Human Disease   ( DOID:0070008 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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