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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (26):

Pheochromocytoma; Carcinoid tumor of intestine; Congenital central hypoventilation more...

Genes (12):

FH (1q43); MAX (14q23.3); MEN1 (11q13.1); NF1 (17q11.2); RET (10q11.21) more...

Conditions

Total conditions: 26

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:

PubMed Clinical Queries

Reviews in PubMed

Suggested reading:

NCI PDQ, Endocrine and Neuroendocrine Neoplasia genetics

NCI PDQ, Cancer Genetics Counseling

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View MAX variations in ClinVar

View RET variations in ClinVar

View VHL variations in ClinVar

View TMEM127 variations in ClinVar

Coriell Institute for Medical Research

Practice guidelines:

Consumer resources:

Genetic Alliance

MedlinePlusGenetics (GHR)

NCATS Office of Rare Diseases Research (GARD)

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.