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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations