OBO ID: DOID:0110346
Term Name: osteogenesis imperfecta type 10 Search Ontology:
Synonyms:
  • OI10
  • osteogenesis imperfecta type X
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/20188343
References:
Ontology: Human Disease   ( DOID:0110346 )
Relationships
is a type of:
OTHER osteogenesis imperfecta type 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SERPINH1 Osteogenesis imperfecta, type X 613848
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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