Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 61395005

SNOMED CT code

SNOMED code

61395005

name

Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia

status

active

date introduced

2002-01-31

fully specified name(s)

Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)

synonyms

Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia
HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia
HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia

attributes - group2

Interprets

Measurement of total hemoglobin concentration 441689006

Has interpretation

Below reference range 281300000

attributes - group3

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Hereditary persistence of fetal hemoglobin thalassemia 16964007
Beta plus thalassemia 79592006

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Thalassemia 40108008
Hereditary persistence of fetal hemoglobin thalassemia 16964007
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 61395005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Thalassemia 40108008
Beta thalassemia 65959000
Beta plus thalassemia 79592006
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 61395005

ancestors

sorted most to least specific

Hereditary persistence of fetal hemoglobin thalassemia 16964007
Beta plus thalassemia 79592006
Beta thalassemia 65959000
Thalassemia 40108008
Anemia due to disturbance of hemoglobin synthesis 14514008
Hereditary hemoglobinopathy 427306008
Hemoglobin below reference range 165397008
Hereditary red blood cell disorder 414394009
Anemia 271737000
Congenital disease 66091009
Hemoglobinopathy 80141007
Hemoglobin level outside reference range 441793007
Red blood cell disorder 38292009
Measurement finding below reference range 442686002
Hereditary disorder of cellular element of blood 414393003
Hemoglobin finding 250220000
Disorder of cellular component of blood 414022008
Measurement finding outside reference range 442096005
Hematology test outside reference range 34641000087106
Hereditary disorder by system 363137000
Hematopoietic system finding 106200001
Disorder of body system 362965005
Finding of blood, lymphatics and immune system 299691001
Protein level - finding 365799007
Hereditary disease 32895009
Finding of substance level 785671009
Genetic disease 782964007
Disease 64572001
Measurement finding 118245000
Evaluation finding 441742003
Procedure related finding 127325009
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Congenital disease 66091009

Hereditary hemoglobinopathy 427306008

Thalassemia 40108008

Hereditary persistence of fetal hemoglobin thalassemia 16964007

Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 61395005

SNOMED CT code