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69981004: Hereditary spherocytosis due to beta spectrin defect (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
116225016 Hereditary spherocytosis due to beta spectrin defect en Synonym Active Case insensitive SNOMED CT core
809986012 Hereditary spherocytosis due to beta spectrin defect (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 spherocytosis due to beta spectrin defect Has interpretation Present true Inferred relationship Some 4
Hereditary spherocytosis due to beta spectrin defect Interprets Haemolysis true Inferred relationship Some 4
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Finding site Entire haematological system false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Finding site Haematopoietic system structure false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Is a Hereditary spherocytosis true Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Is a Disorder of haematopoietic structure true Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Has definitional manifestation Haemolysis false Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocyte true Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Finding site Haematopoietic system structure true Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Has interpretation Below reference range true Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Has interpretation Below reference range true Inferred relationship Some 3
Hereditary spherocytosis due to beta spectrin defect Interprets Red blood cell count true Inferred relationship Some 2
Hereditary spherocytosis due to beta spectrin defect Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 3
Hereditary spherocytosis due to beta spectrin defect Associated morphology Spherocytosis false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Occurrence Congenital false Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Associated morphology Defect false Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Finding site Erythrocyte true Inferred relationship Some 5
Hereditary spherocytosis due to beta spectrin defect Finding site Entire haematological system false Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect 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

Problem/Diagnosis reference set

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