OBO ID: DOID:0070011
Term Name: Seckel syndrome 7 Search Ontology:
Synonyms:
  • SCKL7
Definition: A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/22933543
References:
Ontology: Human Disease   ( DOID:0070011 )
Relationships
is a type of:
OTHER Seckel syndrome 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NIN ?Seckel syndrome 7 614851
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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