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DO Term : autosomal recessive dyskeratosis congenita 6 [DOID:0070024] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the PARN gene on chromosome 16p13.12.
  • synonyms:
  • OMIM:616353,
  • DKCB6,
  • 616353
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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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