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DO Term : nephronophthisis 3 [DOID:0111114] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the NPHP3 gene on chromosome 3q22.
  • synonyms:
  • NPHP3,
  • OMIM:604387,
  • NPH3,
  • MESH:C565780,
  • 604387
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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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