Hemoglobin M disease 74912001

SNOMED CT code

SNOMED code

74912001

name

Hemoglobin M disease

status

active

date introduced

2002-01-31

fully specified name(s)

Hereditary methemoglobinemia due to globin chain mutation (disorder)

synonyms

Hemoglobin M disease
Hereditary M hemoglobinopathy
Hereditary methemoglobinuria
Hereditary methaemoglobinuria
Hereditary methemoglobinemia due to globin chain mutation
Hereditary methemoglobinaemia due to globin chain mutation
Hereditary M haemoglobinopathy
Haemoglobin M disease

attributes - group1

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Hereditary hemoglobinopathy due to globin chain mutation 127038008
Congenital methemoglobinemia 267550008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Hereditary hemoglobinopathy due to globin chain mutation 127038008
Hemoglobin M disease 74912001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital methemoglobinemia 267550008
Hemoglobin M disease 74912001

ancestors

sorted most to least specific

Hereditary hemoglobinopathy due to globin chain mutation 127038008
Congenital methemoglobinemia 267550008
Hereditary hemoglobinopathy 427306008
Methemoglobinemia 38959009
Hereditary red blood cell disorder 414394009
Hemoglobinopathy 80141007
Congenital disease 66091009
Red blood cell disorder 38292009
Hereditary disorder of cellular element of blood 414393003
Hereditary disorder by system 363137000
Disorder of cellular component of blood 414022008
Disorder of body system 362965005
Hereditary disease 32895009
Finding of blood, lymphatics and immune system 299691001
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Congenital disease 66091009

Hereditary hemoglobinopathy 427306008

Hereditary hemoglobinopathy due to globin chain mutation 127038008

Hemoglobin M disease 74912001

SNOMED CT code