FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

44452003: Normocytic hypochromic anemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
493894017 Hypochromic anaemia en Synonym Active Case insensitive SNOMED CT core
493896015 Normocytic hypochromic anaemia en Synonym Active Case insensitive SNOMED CT core
74124013 Normocytic hypochromic anemia en Synonym Active Case insensitive SNOMED CT core
74127018 Hypochromic anemia en Synonym Active Case insensitive SNOMED CT core
781583013 Normocytic hypochromic anemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Normocytic hypochromic anaemia Is a Anaemia true Inferred relationship Some
Normocytic hypochromic anaemia Has definitional manifestation Erythropenia false Inferred relationship Some
Normocytic hypochromic anaemia Finding site Haematopoietic system structure false Inferred relationship Some
Normocytic hypochromic anaemia Has interpretation Below reference range false Inferred relationship Some 1
Normocytic hypochromic anaemia Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
Normocytic hypochromic anaemia Has interpretation Below reference range false Inferred relationship Some 2
Normocytic hypochromic anaemia Interprets Red blood cell count false Inferred relationship Some 2
Normocytic hypochromic anaemia Finding site Haematopoietic system structure false Inferred relationship Some
Normocytic hypochromic anaemia Finding site Erythrocyte false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Idiopathic hypochromic anaemia Is a True Normocytic hypochromic anaemia Inferred relationship Some

Reference Sets

Clinical manifestation reference set

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start