55995005: Hereditary spherocytosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Protein level - finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Red blood cell count outside reference range\RBC count low\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Red blood cell count outside reference range\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\RBC count low\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\RBC count low\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\RBC count low\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Evaluation finding\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary spherocytosis

\Finding of blood, lymphatics and immune system\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Anaemia due to intrinsic red cell abnormality\Anaemia due to membrane defect\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Haemolytic disorder\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Blood disease\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Haemolysis\Haemolytic disorder\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Haemolysis\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis

\Functional finding\Red blood cell destruction finding\Haemolysis\Haemolytic disorder\Haemolytic anaemia\...

\Anaemia due to membrane defect\Hereditary spherocytosis

\Hereditary haemolytic anaemia\Hereditary spherocytosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary spherocytosis
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Blood disease\Anaemia\Anaemia due to intrinsic red cell abnormality\Anaemia due to membrane defect\Hereditary spherocytosis
\Disease\Blood disease\Anaemia\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Disease\Blood disease\Anaemia\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Blood disease\Haemolytic disorder\Haemolytic anaemia\Anaemia due to membrane defect\Hereditary spherocytosis
\Disease\Blood disease\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Blood disease\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary spherocytosis
\Disease\Disorder of body system\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis

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

Descriptions:

Id Description Lang Type Status Case? Module

1231551018 HS - Hereditary spherocytosis en Synonym Active Case sensitive SNOMED CT core
497486018 Congenital spherocytic haemolytic anaemia en Synonym Active Case insensitive SNOMED CT core
794457015 Hereditary spherocytosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
93126010 Hereditary spherocytosis en Synonym Active Case insensitive SNOMED CT core
93127018 Hereditary spherocytosis, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
93128011 Familial spherocytosis en Synonym Active Case insensitive SNOMED CT core
93129015 Minkowsky-Chauffard syndrome en Synonym Active Case sensitive SNOMED CT core
93130013 Congenital spherocytosis en Synonym Active Case insensitive SNOMED CT core
93131012 Familial acholuric jaundice en Synonym Active Case insensitive SNOMED CT core
93132017 Congenital spherocytic hemolytic anemia en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary spherocytosis	Has interpretation	Present	true	Inferred relationship	Some	3
Hereditary spherocytosis	Interprets	Haemolysis	true	Inferred relationship	Some	3
Hereditary spherocytosis	Associated morphology	Spherocyte	false	Inferred relationship	Some	1
Hereditary spherocytosis	Finding site	Entire haematological system	false	Inferred relationship	Some	1
Hereditary spherocytosis	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	1
Hereditary spherocytosis	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Hereditary spherocytosis	Is a	Anaemia due to membrane defect	true	Inferred relationship	Some
Hereditary spherocytosis	Is a	Congenital haemolytic anaemia	false	Inferred relationship	Some
Hereditary spherocytosis	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Hereditary spherocytosis	Is a	Erythrocyte membrane abnormality	true	Inferred relationship	Some
Hereditary spherocytosis	Is a	Hereditary disorder of haematologic system	false	Inferred relationship	Some
Hereditary spherocytosis	Is a	Hereditary haemolytic anaemia	true	Inferred relationship	Some
Hereditary spherocytosis	Has definitional manifestation	Haemolysis	false	Inferred relationship	Some
Hereditary spherocytosis	Associated morphology	Spherocyte	true	Inferred relationship	Some	5
Hereditary spherocytosis	Finding site	Erythrocyte	true	Inferred relationship	Some	4
Hereditary spherocytosis	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary spherocytosis	Has interpretation	Below reference range	true	Inferred relationship	Some	1
Hereditary spherocytosis	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Hereditary spherocytosis	Interprets	Red blood cell count	true	Inferred relationship	Some	1
Hereditary spherocytosis	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Hereditary spherocytosis	Finding site	Entire haematological system	false	Inferred relationship	Some	1
Hereditary spherocytosis	Finding site	Erythrocyte	false	Inferred relationship	Some	1
Hereditary spherocytosis	Associated morphology	Defect	false	Inferred relationship	Some
Hereditary spherocytosis	Occurrence	Congenital	false	Inferred relationship	Some
Hereditary spherocytosis	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Hereditary spherocytosis	Associated morphology	Spherocytosis	false	Inferred relationship	Some	1
Hereditary spherocytosis	Interprets	Erythrocyte destruction	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Whole blood screening of hereditary spherocytosis using flow cytometry	Has focus	False	Hereditary spherocytosis	Inferred relationship	Some
Whole blood screening of hereditary spherocytosis using flow cytometry	Has focus	True	Hereditary spherocytosis	Inferred relationship	Some	892540153
Hereditary spherocytosis due to spectrin deficiency	Is a	True	Hereditary spherocytosis	Inferred relationship	Some
Hereditary spherocytosis due to deficiency of protein 4.2	Is a	True	Hereditary spherocytosis	Inferred relationship	Some
Hereditary spherocytosis due to beta spectrin defect	Is a	True	Hereditary spherocytosis	Inferred relationship	Some
FH: Hereditary spherocytosis	Associated finding	True	Hereditary spherocytosis	Inferred relationship	Some	1
FH: Hereditary spherocytosis	Associated finding	False	Hereditary spherocytosis	Inferred relationship	Some	1
FH: Spherocytosis	Associated finding	False	Hereditary spherocytosis	Inferred relationship	Some	1
FH: Spherocytosis	Associated finding	True	Hereditary spherocytosis	Inferred relationship	Some	1
FH: Hereditary spherocytosis	Associated finding	False	Hereditary spherocytosis	Inferred relationship	Some	1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1231551018	HS - Hereditary spherocytosis	en	Synonym	Active	Case sensitive	SNOMED CT core
497486018	Congenital spherocytic haemolytic anaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
794457015	Hereditary spherocytosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
93126010	Hereditary spherocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
93127018	Hereditary spherocytosis, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
93128011	Familial spherocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
93129015	Minkowsky-Chauffard syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
93130013	Congenital spherocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
93131012	Familial acholuric jaundice	en	Synonym	Active	Case insensitive	SNOMED CT core
93132017	Congenital spherocytic hemolytic anemia	en	Synonym	Active	Case insensitive	SNOMED CT core