OBO ID: DOID:0070008
Term Name: Seckel syndrome 10 Search Ontology:
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 Seckel syndrome 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NSMCE2 Seckel syndrome 10 617253
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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