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DO Term : Bardet-Biedl syndrome 9 [DOID:0110131] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Bardet-Biedl syndrome that has_material_basis_in homozygosity or compound heterozygosity for mutations in the PTHB1 gene on chromosome 7p14.
  • synonyms:
  • 615986,
  • OMIM:615986,
  • BBS9,
  • GARD:10208,
  • MESH:C565918,
  • ICD10CM:Q87.89
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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