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1153399000: Homozygous hereditary elliptocytosis (disorder)


Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4564212016 Homozygous hereditary elliptocytosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4564213014 Homozygous hereditary elliptocytosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous hereditary elliptocytosis Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 3
Homozygous hereditary elliptocytosis Has interpretation Below reference range true Inferred relationship Some 3
Homozygous hereditary elliptocytosis Associated morphology Elliptocyte true Inferred relationship Some 1
Homozygous hereditary elliptocytosis Finding site Erythrocyte true Inferred relationship Some 1
Homozygous hereditary elliptocytosis Interprets Haemolysis true Inferred relationship Some 4
Homozygous hereditary elliptocytosis Is a Hereditary elliptocytosis true Inferred relationship Some
Homozygous hereditary elliptocytosis Interprets Red blood cell count true Inferred relationship Some 2
Homozygous hereditary elliptocytosis Pathological process Pathological developmental process true Inferred relationship Some 1
Homozygous hereditary elliptocytosis Occurrence Congenital true Inferred relationship Some 1
Homozygous hereditary elliptocytosis Has interpretation Present true Inferred relationship Some 4
Homozygous hereditary elliptocytosis Has interpretation Below reference range true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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