OBO ID: DOID:0070012 |
Term Name: | Seckel syndrome 5 | Search Ontology: | |
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Definition: | A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/21131973 | ||
References: | |||
Ontology: | Human Disease ( DOID:0070012 ) |
OTHER Seckel syndrome 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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