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DO Term : reticular dysgenesis [DOID:0060020] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A severe combined immunodeficiency that is the most severe form of SCID and has_material_basis_in mutations in the gene encoding mitochondrial adenylate kinase 2. It is characterized by congenital agranulocytosis, lymphopenia, and lymphoid and thymic hypoplasia with absent cellular and humoral immunity functions.
  • synonyms:
  • MESH:C538361,
  • GARD:8625,
  • OMIM:267500,
  • aleukocytosis,
  • DOID:1226,
  • De Vaal disease,
  • UMLS_CUI:C0272167,
  • 267500,
  • SNOMEDCT_US_2023_03_01:111584000,
  • NCI:C27070
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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