Clinical and research tests for Meningitis - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 6298	Meningitis	Meningitis (disease)
Select item 45811	Familial Mediterranean fever	Benign paroxysmal peritonitis Familial Mediterranean Fever Type 1 Familial Mediterranean Fever Type 2 POLYSEROSITIS, FAMILIAL PAROXYSMAL POLYSEROSITIS, RECURRENT Periodic disease Periodic peritonitis
Select item 65123	X-linked agammaglobulinemia	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1 Agammaglobulinemia, BTK Agammaglobulinemia, Bruton tyrosine kinase BTK-deficiency Bruton's agammaglobulinemia Bruton-type agammaglobulinemia IMMUNODEFICIENCY 1
Select item 341987	Familial Mediterranean fever, autosomal dominant	Dominant Familial Mediterranean Fever FMF, AUTOSOMAL DOMINANT
Select item 1647324	Familial cold autoinflammatory syndrome 1	CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 1 Familial cold inflammatory syndrome 1
Select item 355270	Complement component 7 deficiency	C7 DEFICIENCY
Select item 325455	Sacral defect with anterior meningocele
Select item 924576	MIRAGE syndrome	MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY
Select item 375137	Immunodeficiency 67	IRAK4 deficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Interleukin receptor-associated kinase deficiency
Select item 462431	Type I complement component 8 deficiency	C8 alpha-gamma deficiency C8 deficiency type I C81 deficiency C8AG DEFICIENCY COMPLEMENT C8 DEFICIENCY, TYPE I Complement component 8 deficiency type 1
Select item 462430	Type II complement component 8 deficiency	C8 beta deficiency C8 deficiency type II C8B DEFICIENCY COMPLEMENT C8 DEFICIENCY, TYPE II COMPLEMENT COMPONENT 8B DEFICIENCY Complement component 8 deficiency type 2 Human complement C8-beta deficiency
Select item 57546	Syphilitic meningitis	Meningeal syphilis Syphilitic aseptic meningitis
Select item 6299	Meningococcal meningitis
Select item 7471	Paroxysmal nocturnal hemoglobinuria	Acquired paroxysmal nocturnal hemoglobinuria
Select item 383023	Pyogenic bacterial infections due to MyD88 deficiency	Myd88 deficiency PYOGENIC BACTERIAL INFECTIONS, RECURRENT, DUE TO MYD88 DEFICIENCY
Select item 39048	Bacterial meningitis
Select item 44354	Pneumococcal meningitis
Select item 1749856	Immunodeficiency 72 with autoinflammation	IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION AND LYMPHOPROLIFERATION
Select item 155889	West-Nile encephalitis
Select item 9788	Listeriosis	Listeria infection

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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.