Fanconi Anemia, Complementation Group W; Fancw

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Fanconi Anemia, Complementation Group W; Fancw

RFWD3

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Fanconi Anemia, Complementation Group W; Fancw

Microcephaly
Growth delay
Anemia
Intrauterine growth retardation
Ventriculomegaly
Midface retrusion
Growth hormone deficiency
Arnold-Chiari malformation
Hypoplasia of the radius
Myelodysplasia

And another 6 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Fanconi Anemia, Complementation Group W; Fancw Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NGS Panel for Fanconi anemia. By BLOODGENETICS BLOODGENETICS (Spain). BRCA1, BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2 , (...) View the complete list with 2 more genes Panel complete gene list BRCA1, BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, RAD51, RAD51C Specificity 5 % Genes 100 %
RFWD3. By Fulgent Genetics Fulgent Genetics (United States). RFWD3 Specificity 100 % Genes 100 %
Fanconi Anemia: gene sequencing panel. By CEN4GEN Institute for Genomics and Molecular Diagnostics (Canada). BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, RAD51 , (...) View the complete list with 1 more genes Panel complete gene list BRCA2, XRCC2, BRIP1, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, RAD51, RAD51C Specificity 5 % Genes 100 %
Esophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel. By CEN4GEN Institute for Genomics and Molecular Diagnostics (Canada). BRCA2, SOX2, XRCC2, BRIP1, CHD7, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG , (...) View the complete list with 4 more genes Panel complete gene list BRCA2, SOX2, XRCC2, BRIP1, CHD7, FANCL, FANCM, SLX4, UBE2T, RFWD3, FANCI, PALB2, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, MAD2L2, MYCN, RAD51, RAD51C Specificity 5 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

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