Fanconi anemia of complementation group C 1285021005
SNOMED CT code
SNOMED code | 1285021005 |
---|---|
name | Fanconi anemia of complementation group C |
status | active |
date introduced | 2023-06-30 |
fully specified name(s) | Fanconi anemia of complementation group C (disorder) |
synonyms |
|
attributes - group6 | |
Due to | Decreased erythrocyte production 18469004 |
attributes - group8 | |
Pathological process | Abnormal immune process 769247005 |
attributes - group2 | |
Interprets | Red blood cell count 14089001 |
Has interpretation | Below reference range 281300000 |
attributes - group3 | |
Interprets | Measurement of total hemoglobin concentration 441689006 |
Has interpretation | Below reference range 281300000 |
attributes - group4 | |
Interprets | Platelet count 61928009 |
Has interpretation | Below reference range 281300000 |
attributes - group5 | |
Interprets | White blood cell count 767002 |
Has interpretation | Below reference range 281300000 |
attributes - group7 | |
Interprets | Hemostatic function 74848003 |
Has interpretation | Abnormal 263654008 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Bone marrow structure 14016003 |
Associated morphology | Aplasia 45486003 |
Pathological process | Pathological developmental process 308490002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Fanconi's anemia 30575002 Fanconi anemia of complementation group C 1285021005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Fanconi anemia of complementation group C 1285021005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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