X chromosome-linked pyridoxine responsive sideroblastic anemia 25443007

SNOMED CT code

SNOMED code

25443007

name

X chromosome-linked pyridoxine responsive sideroblastic anemia

status

active

date introduced

2002-01-31

fully specified name(s)

X chromosome-linked pyridoxine responsive sideroblastic anemia (disorder)

synonyms

X chromosome-linked pyridoxine responsive sideroblastic anemia
Pyridoxine responsive sideroblastic anemia
X chromosome-linked pyridoxine responsive sideroblastic anaemia
Pyridoxine responsive sideroblastic anaemia

attributes - group1

Has interpretation

Below reference range 281300000

Interprets

Measurement of total hemoglobin concentration 441689006

attributes - group2

Has interpretation

Below reference range 281300000

Interprets

Red blood cell count 14089001

attributes - group3

Finding site

Erythrocyte 41898006

Occurrence

Congenital 255399007

parents

X chromosome-linked sideroblastic anemia 48983004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital anemia 63565007
X chromosome-linked sideroblastic anemia 48983004
X chromosome-linked pyridoxine responsive sideroblastic anemia 25443007

ancestors

sorted most to least specific

X chromosome-linked sideroblastic anemia 48983004
X-linked recessive hereditary disease 1162976004
Inherited disorder of porphyrin metabolism 403832004
Hereditary red blood cell disorder 414394009
Sideroblastic anemia 41841004
Congenital anemia 63565007
X-linked hereditary disease 128430005
Hereditary metabolic disease 1821000146108
Red blood cell disorder 38292009
Anemia 271737000
Hemoglobin below reference range 165397008
Disorder of porphyrin metabolism 29094004
Hereditary disorder of cellular element of blood 414393003
Red blood cell count below reference range 165423001
Congenital disease 66091009
Sex-linked hereditary disorder 82852009
Disorder of cellular component of blood 414022008
Hemoglobin level outside reference range 441793007
Metabolic disease 75934005
Hereditary disorder by system 363137000
Red blood cell count outside reference range 165427000
Cytopenia 50820005
Hereditary disease 32895009
Disorder of body system 362965005
Finding of blood, lymphatics and immune system 299691001
Hemoglobin finding 250220000
Red blood cell count - finding 365625004
Measurement finding below reference range 442686002
Hematology test outside reference range 34641000087106
Blood cell count outside reference range 762656009
Genetic disease 782964007
Hematopoietic system finding 106200001
Measurement finding outside reference range 442096005
Protein level - finding 365799007
Disease 64572001
Finding of substance level 785671009
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

Disease 64572001

Congenital disease 66091009

Congenital anemia 63565007

X chromosome-linked sideroblastic anemia 48983004

X chromosome-linked pyridoxine responsive sideroblastic anemia 25443007

SNOMED CT code