Search Ontology:
Human Disease

Seckel syndrome 7

Term ID
DOID:0070011
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 Pages
Genes Involved
Zebrafish Models