T-cell immunodeficiency with epidermodysplasia verruciformis 770785002
SNOMED CT code
SNOMED code | 770785002 |
---|---|
name | T-cell immunodeficiency with epidermodysplasia verruciformis |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | T-cell immunodeficiency due to ras homolog family member H deficiency (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Abnormal immune process 769247005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 T-cell immunodeficiency with epidermodysplasia verruciformis 770785002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 T-cell immunodeficiency with epidermodysplasia verruciformis 770785002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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