OMOP Concept 4006469

Reticular dysgenesis

StandardConditionSNOMED111584000Disorder
Maps from
3
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

3 source codes normalize to Reticular dysgenesis via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL127578Reticular dysgenesisNon-standard
MeSHC538361Reticular dysgenesisNon-standard
Nebraska Lexicon111584000Severe combined immunodeficiency, neutropaenia and thrombocytopaeniaNon-standard

Synonyms

Alternative names recorded for Reticular dysgenesis across source vocabularies.

  • aleuquia congénita
  • Congenital aleukia
  • De Vaal disease
  • disgenesia reticular
  • disgenesia reticular (trastorno)
  • Generalised haematopoietic hypoplasia
  • Generalized hematopoietic hypoplasia
  • Immunoerythromyeloid hypoplasia
  • Reticular dysgenesia
  • Reticular dysgenesis (disorder)
  • SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia
  • Severe combined immunodeficiency, neutropaenia and thrombocytopaenia
  • Severe combined immunodeficiency, neutropenia and thrombocytopenia

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Broader concepts

(44)

Roll up to these when you need a wider cohort.

Narrower concepts

(2)

Included automatically when you query with descendants.

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