Test Entry - Detail

Primary Immunodeficiency Associated Genes

General

Clinical Use:

The Primary Immunodeficiency Associated Gene Panel (PID) consists of up to 474 individual genes.
The Primary Immunodeficiency panel analyses genes that are associated with primary immunodeficiencies including but not limited to antibody deficiencies, autoinflammatory syndromes, disorders of innate immunity, immune dysregulation and phagocytic defects.
If ordering via CPOE (ICM) please request "Immunogenetics Rare Disease Testing".

Availability:

Samples are processed by FSH Immunology and then forwarded to external laboratories for testing.

Aliases/Synonyms:

Antibody Deficiencies (Genetic), Autoinflammatory Disease Gene Panel, Blau Syndrome, Common Variable Immunodeficiency Syndrome, Complement Deficiency (Genetic), CVID, Hyper IgE, Immune Disregulation, Immunodysregulation Polyendocrinopathy Enteropathy X-Linked, IPEX, NOD2, Primary Immunodeficiency Syndrome, Pyogenic Sterile Arthritis with Pyoderma Gangraenosum and Acne, SCID, Severe Combined Immunodeficiency Syndrome,

Code:

IIRD

Handling Instructions (to laboratory):

Send sample ambient.

Hyperlink:

Reference Interval:

Refer to report or laboratory

Collection Requirements

Container:

EDTA (LAV9),

Sample Type:

See container

Minimum Collection Volume:

9mL

Collection Instructions:

Smaller collection volumes acceptable for paediatric patients with buccal and saliva collection kits also available from testing laboratory.
Non-medicare rebateable item. All patients except Public, VA and Pensioners will be billed by external provider.

Processing Requirements

Alternate Containers:

EDTA x 2 (LAVENDER)

Processing Instructions:

Minimum Assay Volume:

9mL

Stability:

Transport Instructions (to testing laboratory):

Send sample ambient.

Testing Locations

Performed at:

Section	Department	Site	Contact Phone
Immunogenetics Molecular	Immunology	Fiona Stanley Hospital	6152 8006

Last Updated : 14-03-2024 08:50