FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

127040003: Sickle cell-hemoglobin SS disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
328014 Sickle cell anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206337013 Hemoglobin S-S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206338015 Drepanocythemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474021015 Drepanocythaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474022010 Sickle cell anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474023017 Haemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474024011 Haemoglobin S-S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474025012 Hemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474026013 Hb S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2547671019 Hb SS disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2663794019 Hereditary hemoglobinopathy disorder homozygous for hemoglobin S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688057012 Sickle cell-hemoglobin SS disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688058019 Sickle cell-haemoglobin SS disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688059010 Sickle cell-hemoglobin SS disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3780079019 Hereditary haemoglobinopathy disorder homozygous for haemoglobin S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
328014 Sickle cell anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
328014 Sickle cell anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206336016 Sickle cell disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206337013 Hemoglobin S-S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
206337013 Hemoglobin S-S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206338015 Drepanocythemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206338015 Drepanocythemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474021015 Drepanocythaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474021015 Drepanocythaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474022010 Sickle cell anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474022010 Sickle cell anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474023017 Haemoglobin S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474023017 Haemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474024011 Haemoglobin S-S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474024011 Haemoglobin S-S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474024011 Haemoglobin S-S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474025012 Hemoglobin S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474025012 Hemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474026013 Hb S disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474027016 Sickle cell syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
731078012 Hereditary hemoglobinopathy disorder homozygous for hemoglobin S (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2547671019 Hb SS disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2547671019 Hb SS disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2663794019 Hereditary hemoglobinopathy disorder homozygous for hemoglobin S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688057012 Sickle cell-hemoglobin SS disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688058019 Sickle cell-haemoglobin SS disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3688059010 Sickle cell-hemoglobin SS disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3780079019 Hereditary haemoglobinopathy disorder homozygous for haemoglobin S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
384281000274110 Sichelzellanämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440831001000119 Sichelzellkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
440781000172118 drépanocytose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
440781000172118 drépanocytose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
384281000274110 Sichelzellanämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440831001000119 Sichelzellkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hb S disease Is a Haemoglobinopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a Anaemia false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Causative agent (attribute) Haemoglobin S true Inferred relationship Existential restriction modifier (core metadata concept) 5
Hb S disease Associated morphology Drepanocyte (cell) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hb S disease Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hb S disease Is a Anaemia due to disturbance of haemoglobin synthesis true Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hb S disease Is a trouble causé par un médicament false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a trouble selon la localisation corporelle false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Finding site Erythroid cell (cell) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hb S disease Is a Sickling disorder due to hemoglobin S (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a Homozygous haemoglobinopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Is a anémie causée par une substance false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hb S disease Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hb S disease Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hb S disease Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hb S disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hb S disease Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hb S disease Is a Congenital anemia false Inferred relationship Existential restriction modifier (core metadata concept)
Hb S disease Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Sickle cell anemia with high hemoglobin F Is a True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell retinopathy Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-haemoglobin Lepore disease Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-Hemoglobin O Arab disease Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin S disease without crisis Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin D disease (disorder) Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin C disease Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-thalassemia disease Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin E disease Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin S disease with crisis Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell anemia with no crisis Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell anemia with crisis Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell anemia of unspecified type Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell anemia NOS Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
[X]Other sickle cell disorders Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell nephropathy Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Hand-foot syndrome in sickle cell anemia (disorder) Is a False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history of sickle cell anemia Associated finding False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute chest syndrome After True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Hemoglobin SS disease with crisis Is a True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Haemoglobin SS disease without crisis Is a True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell anemia with coexistent alpha-thalassemia Is a True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin C retinopathy Due to False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 3
Sickle cell retinopathy Due to False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2
Proliferative retinopathy due to sickle cell disease Due to True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2
Antenatal sickle cell screening (procedure) Has focus False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of sickle cell anemia Associated finding True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Screening for sickle cell disease (procedure) Has focus True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2
Antenatal sickle cell screening (procedure) Has focus True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2
History of sickle cell anemia (situation) Associated finding False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
History of sickle cell anemia (situation) Associated finding True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of sickle cell anemia Associated finding False Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Sickle cell anemia in mother complicating childbirth Is a True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept)
Acute chest syndrome due to sickle cell thalassaemia with crisis After True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2
Acute chest syndrome due to sickle cell haemoglobin C disease with crisis After True Hb S disease Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

Back to Start