Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT code

SNOMED code

5300004

name

Hemoglobin Bart's hydrops syndrome

status

active

date introduced

2002-01-31

fully specified name(s)

Hemoglobin Bart's hydrops syndrome (disorder)

synonyms

Haemoglobin Bart hydrops syndrome
Hemoglobin Bart hydrops syndrome
Alpha thalassemia major
Hemoglobin Barts hydrops
Haemoglobin Bart's hydrops syndrome
Alpha thalassaemia major
Haemoglobin Bart's disease
Haemoglobin Barts hydrops
Hemoglobin Bart's hydrops syndrome
Hemoglobin Bart's disease

attributes - group4

Occurrence

Fetal period 303112003

Associated morphology

Hydrops 20741006

attributes - group1

Has interpretation

Below reference range 281300000

Interprets

Red blood cell count 14089001

attributes - group2

Has interpretation

Below reference range 281300000

Interprets

Measurement of total hemoglobin concentration 441689006

attributes - group3

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Fetus with hereditary disease 199531009
Hydrops fetalis 276508000
Fetal anemia 462166006
Congenital anemia 63565007
Alpha thalassemia 68913001
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Fetal finding 106112009
Fetal disorder 70591005
Fetus with hereditary disease 199531009
Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT Concept 138875005
Clinical finding 404684003
Edema 267038008
Disorder characterized by edema 118654009
Hydrops fetalis 276508000
Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT Concept 138875005
Clinical finding 404684003
Fetal finding 106112009
Fetal disorder 70591005
Fetal anemia 462166006
Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital anemia 63565007
Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Thalassemia 40108008
Alpha thalassemia 68913001
Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Hemoglobin Bart's hydrops syndrome 5300004

ancestors

sorted most to least specific

Fetus with hereditary disease 199531009
Hydrops fetalis 276508000
Fetal anemia 462166006
Congenital anemia 63565007
Alpha thalassemia 68913001
Autosomal recessive hereditary disorder 85995004
Disorder characterized by edema 118654009
Thalassemia 40108008
Autosomal hereditary disorder 1899006
Fetal disorder 70591005
Red blood cell count below reference range 165423001
Edema 267038008
Anemia due to disturbance of hemoglobin synthesis 14514008
Fetal finding 106112009
Red blood cell count outside reference range 165427000
Hereditary hemoglobinopathy 427306008
Disorder of fetus and/or newborn 414025005
Cytopenia 50820005
Anemia 271737000
Hemoglobin below reference range 165397008
Red blood cell count - finding 365625004
Congenital disease 66091009
Hereditary red blood cell disorder 414394009
Blood cell count outside reference range 762656009
Hemoglobinopathy 80141007
Hemoglobin level outside reference range 441793007
Measurement finding below reference range 442686002
Red blood cell disorder 38292009
Hereditary disorder of cellular element of blood 414393003
Disorder of cellular component of blood 414022008
Hemoglobin finding 250220000
Measurement finding outside reference range 442096005
Hematology test outside reference range 34641000087106
Hereditary disorder by system 363137000
Hereditary disease 32895009
Finding of blood, lymphatics and immune system 299691001
Hematopoietic system finding 106200001
Protein level - finding 365799007
Disorder of body system 362965005
Genetic disease 782964007
Finding of substance level 785671009
Disease 64572001
Measurement finding 118245000
Evaluation finding 441742003
Procedure related finding 127325009
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Fetal finding 106112009

Fetal disorder 70591005

Fetus with hereditary disease 199531009

Hemoglobin Bart's hydrops syndrome 5300004

SNOMED CT code