44641000: Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\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 enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\RBC count low\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\RBC count low\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\RBC count low\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\RBC count low\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency

\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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Anaemia due to metabolic disorder\Anaemia due to enzymopathy\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Haemolytic disorder\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Blood disease\Red blood cell disorder\Erythrocyte enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Haemolysis\Haemolytic disorder\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Haemolysis\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency

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

\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency

\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency

\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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Anaemia\Anaemia due to metabolic disorder\Anaemia due to enzymopathy\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Anaemia\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Anaemia\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Haemolytic disorder\Haemolytic anaemia\Anaemia due to enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Haemolytic disorder\Haemolytic anaemia\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Blood disease\Red blood cell disorder\Erythrocyte enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency
\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 nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemolytic anaemia\Hereditary nonspherocytic haemolytic anaemia\HNSHA due to triosephosphate isomerase deficiency
\Disease\Disorder of body system\Red blood cell disorder\Erythrocyte enzyme deficiency\HNSHA due to triosephosphate isomerase deficiency

Status: current, Defined. Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2620827010 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

2620828017 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency en Synonym Active Initial character case insensitive SNOMED CT core

2914313017 Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core

2914791016 Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency en Synonym Active Case insensitive SNOMED CT core

3780589014 Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency en Synonym Active Case insensitive SNOMED CT core

493971019 Triosephosphate deficiency anaemia en Synonym Active Case insensitive SNOMED CT core

74466015 HNSHA due to triosephosphate isomerase deficiency en Synonym Active Case sensitive SNOMED CT core

74467012 Triosephosphate deficiency anemia en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
HNSHA due to triosephosphate isomerase deficiency	Has interpretation	Present	true	Inferred relationship	Some	3
HNSHA due to triosephosphate isomerase deficiency	Interprets	Haemolysis	true	Inferred relationship	Some	3
HNSHA due to triosephosphate isomerase deficiency	Is a	Hereditary nonspherocytic haemolytic anaemia	true	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Associated etiologic finding	Enzymopathy	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Associated etiologic finding	Triose phosphate isomerase deficiency	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Anaemia due to enzyme deficiency	true	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Inborn error of metabolism	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Hereditary disorder of haematologic system	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Erythrocyte enzyme deficiency	true	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Due to	Triose phosphate isomerase deficiency	true	Inferred relationship	Some	5
HNSHA due to triosephosphate isomerase deficiency	Finding site	Body system structure	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Has definitional manifestation	Haemolysis	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Has interpretation	Below reference range	true	Inferred relationship	Some	1
HNSHA due to triosephosphate isomerase deficiency	Interprets	Red blood cell count	true	Inferred relationship	Some	1
HNSHA due to triosephosphate isomerase deficiency	Has interpretation	Below reference range	true	Inferred relationship	Some	2
HNSHA due to triosephosphate isomerase deficiency	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
HNSHA due to triosephosphate isomerase deficiency	Finding site	Erythrocyte	true	Inferred relationship	Some	4
HNSHA due to triosephosphate isomerase deficiency	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Occurrence	Congenital	false	Inferred relationship	Some
HNSHA due to triosephosphate isomerase deficiency	Interprets	Erythrocyte destruction	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2620827010	Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2620828017	Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2914313017	Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2914791016	Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3780589014	Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
493971019	Triosephosphate deficiency anaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
74466015	HNSHA due to triosephosphate isomerase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
74467012	Triosephosphate deficiency anemia	en	Synonym	Active	Case insensitive	SNOMED CT core