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DO Term : Fraser syndrome 2 [DOID:0111407] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3.
  • synonyms:
  • FRASRS2,
  • 617666,
  • OMIM:617666
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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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