OBO ID: DOID:0070013
Term Name: Seckel syndrome 2 Search Ontology:
Synonyms:
  • microcephalic primordial dwarfism 2
  • SCKL2
  • Seckel-type dwarfism 2
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the RBBP8 gene on chromosome 18q11. https://www.ncbi.nlm.nih.gov/pubmed/21998596
References:
Ontology: Human Disease   ( DOID:0070013 )
Relationships
is a type of:
OTHER Seckel syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RBBP8 Seckel syndrome 2 606744
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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