- Unknown type - GTR

Genetic Testing Registry

View Advanced Search Options

Classic view of this page

see more see less

Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (7):

X-linked lymphoproliferative disease due to XIAP deficiency; Familial hemophagocytic lymphohistiocytosis 2; Familial hemophagocytic lymphohistiocytosis 3 more...

Genes (41):

ADA (20q13.12); AP3B1 (5q14.1); AP3D1 (19p13.3); CD27 (12p13.31); CD70 (19p13.3) more...

Conditions

Total conditions: 7

Condition/Phenotype	Identifier

Methodology

Total methods: 0

Method Category

Test method

Instrument *

* Instrument: Not provided

Technical Information

Recommended fields not provided:

Test Confirmation

Additional Information

Reviews:

Genereviews

PubMed Clinical Queries

Clinical resources:

Molecular resources:

View XIAP variations in ClinVar

RefSeqGene

Coriell Institute for Medical Research

Consumer resources:

Genetic Alliance

MalaCards

MedlinePlusGenetics (GHR)

NCATS Office of Rare Diseases Research (GARD)

MedlinePlus

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in 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.