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DO Term : nephrotic syndrome type 11 [DOID:0080385] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15.
  • synonyms:
  • 616730,
  • OMIM:616730
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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