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75443009: Hereditary elliptocytosis due to abnormal protein 4.1 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym Active Case insensitive SNOMED CT core
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Haemolysis true Inferred relationship Some 3
Hereditary elliptocytosis due to abnormal protein 4.1 Occurrence Congenital true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Pathological process Pathological developmental process true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Associated morphology Elliptocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Present true Inferred relationship Some 3
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary elliptocytosis true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary disorder of haematologic system false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Body system structure false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Some 1
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 1
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Some 2
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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