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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (6):

Holoprosencephaly sequence; Holoprosencephaly 2; Holoprosencephaly 3 more...

Genes (11):

DISP1 (1q41); FGF8 (10q24.32); FOXH1 (8q24.3); GLI2 (2q14.2); NODAL (10q22.1) more...

Conditions

Total conditions: 6

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

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View NODAL variations in ClinVar

View FOXH1 variations in ClinVar

Practice guidelines:

EuroGenetest, 2011

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.