Poikiloderma with neutropenia 772126000
SNOMED CT code
SNOMED code | 772126000 |
---|---|
name | Poikiloderma with neutropenia |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Poikiloderma with neutropenia (disorder) |
synonyms |
|
attributes - group2 | |
Finding site | Skin structure 39937001 |
Associated morphology | Poikiloderma 70114006 |
attributes - group3 | |
Clinical course | Chronic 90734009 |
attributes - group1 | |
Interprets | Neutrophil count 30630007 |
Has interpretation | Below reference range 281300000 |
attributes - group4 | |
Pathological process | Abnormal immune process 769247005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of skin 128236002 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 White blood cell disorder 54097007 Leukopenia 84828003 Neutropenic disorder 303011007 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Atrophic condition of skin 400190005 Poikiloderma 402685001 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of immune function 413834006 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 White blood cell disorder 54097007 Hereditary white blood cell disorder 414395005 Poikiloderma with neutropenia 772126000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Poikiloderma with neutropenia 772126000 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.