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DO Term : autosomal recessive congenital bilateral absence of vas deferens [DOID:0111864] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2.
  • synonyms:
  • 277180,
  • OMIM:277180
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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