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154801000: (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) (disorder)

  • (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism)

Status: retired, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
240761012 (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) en Synonym Active Initial character case insensitive SNOMED CT core
240762017 (Hereditary: [elliptocytosis] or [stomatocytosis] or [other hemalytic anemias]) or (favism) en Synonym Active Initial character case insensitive SNOMED CT core
240763010 Favism en Synonym Active Case insensitive SNOMED CT core
240764016 Hereditary stomatocytosis en Synonym Active Case insensitive SNOMED CT core
240765015 Hereditary elliptocytosis en Synonym Active Case insensitive SNOMED CT core
240766019 Other hered. hem. anemias en Synonym Active Case insensitive SNOMED CT core
240767011 Other hered. haem. anaemias en Synonym Active Case insensitive SNOMED CT core
2715414019 (Hereditary: [elliptocytosis] or [stomatocytosis] or [other haemalytic anaemias]) or (favism) (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian dialect reference set

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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