T-cell immunodeficiency with epidermodysplasia verruciformis   770785002

SNOMED CT code


SNOMED code770785002
nameT-cell immunodeficiency with epidermodysplasia verruciformis
statusactive
date introduced2019-01-31
fully specified name(s)T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)
synonyms
  • T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency
  • T-cell immunodeficiency with epidermodysplasia verruciformis
  • T-cell immunodeficiency due to RHOH deficiency
  • T-cell immunodeficiency due to ras homolog family member H deficiency
attributes - group1
Pathological processAbnormal immune process   769247005
parents
  • Primary immune deficiency disorder   58606001
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical 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

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