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191182000: (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary) (disorder)

  • (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary)

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

Descriptions:

Id Description Lang Type Status Case? Module
2755178017 (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary) (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
294008015 (Thalassaemia (& Mediterranean anaemia)) or (leptocytosis, hereditary) en Synonym Active Initial character case insensitive SNOMED CT core
294009011 Mediterranean anemia en Synonym Active Case sensitive SNOMED CT core
294010018 Thalassemia en Synonym Active Case insensitive SNOMED CT core
294011019 Mediterranean anaemia en Synonym Active Case sensitive SNOMED CT core
294012014 Thalassaemia en Synonym Active Case insensitive SNOMED CT core
294013016 Leptocytosis, hereditary en Synonym Active Case insensitive SNOMED CT core
294014010 (Thalassemia (& Mediterranean anemia)) or (leptocytosis, hereditary) en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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