770785002: T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\T-cell immunodeficiency with epidermodysplasia verruciformis
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\T-cell immunodeficiency with epidermodysplasia verruciformis

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3702782013	T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
3702783015	T-cell immunodeficiency with epidermodysplasia verruciformis	en	Synonym	Active	Case sensitive	SNOMED CT core
3702784014	T-cell immunodeficiency due to RHOH deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
3702786011	T-cell immunodeficiency due to ras homolog family member H deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
3702787019	T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3702785010	A rare primary immunodeficiency with characteristics of increased susceptibility to infection by human papillomavirus, presenting in childhood with disseminated flat wart-like cutaneous lesions. Burkitt lymphoma has also been reported. Whilst total T-cell counts are normal, there is impaired TCR signaling, profound peripheral naive T-cell lymphopenia with memory T-cells displaying an exhaustion phenotype.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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