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17235000: Spherocytosis (finding)


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

Descriptions:

Id Description Lang Type Status Case? Module
29144019 Spherocytosis en Synonym Active Case insensitive SNOMED CT core
744410015 Spherocytosis (finding) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spherocytosis Interprets Haematology procedure true Inferred relationship Some 3
Spherocytosis Interprets Red blood cell shape true Inferred relationship Some 2
Spherocytosis Is a Finding of red blood cell shape true Inferred relationship Some
Spherocytosis Associated morphology Spherocyte true Inferred relationship Some 1
Spherocytosis Finding site Erythrocyte false Inferred relationship Some
Spherocytosis Interprets Laboratory test false Inferred relationship Some
Spherocytosis Finding method Procedure false Inferred relationship Some
Spherocytosis Interprets Red blood cell morphology false Inferred relationship Some 2
Spherocytosis Finding site Haematopoietic system structure false Inferred relationship Some
Spherocytosis Interprets Red blood cell shape false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Associated morphology False Spherocytosis Inferred relationship Some 1
FH: Spherocytosis Associated finding False Spherocytosis Inferred relationship Some 1
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Associated morphology False Spherocytosis Inferred relationship Some 1
Mild hereditary spherocytosis due to spectrin deficiency Associated morphology False Spherocytosis Inferred relationship Some 1
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Associated morphology False Spherocytosis Inferred relationship Some 1
Severe hereditary spherocytosis due to spectrin deficiency Associated morphology False Spherocytosis Inferred relationship Some 1
Hereditary spherocytosis due to spectrin deficiency Associated morphology False Spherocytosis Inferred relationship Some 1
Hereditary spherocytosis due to deficiency of protein 4.2 Associated morphology False Spherocytosis Inferred relationship Some 1
Hereditary spherocytosis Associated morphology False Spherocytosis Inferred relationship Some 1
Hereditary spherocytosis due to beta spectrin defect Associated morphology False Spherocytosis Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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