Thrombophilia, X-linked, Due To Factor Ix Defect; Thph8

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 Thrombophilia, X-linked, Due To Factor Ix Defect; Thph8

Clinical Features

Phenotypes and symptoms related to Thrombophilia, X-linked, Due To Factor Ix Defect; Thph8

Venous thrombosis
Deep venous thrombosis
Hypercoagulability
Abnormality of the intrinsic pathway

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.

Thrombophilia, X-linked, Due To Factor Ix Defect; Thph8 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Factor IX full gene sequencing. By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center (United States). F9 Specificity 100 % Genes 100 %
DNA Hemophilia B Mutation Evaluation. By Genomics - Bleeding Disorders BloodworksNW (United States). F9 Specificity 100 % Genes 100 %
Hemophilia B. By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine (United States). F9 Specificity 100 % Genes 100 %
F9 Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). F9 Specificity 100 % Genes 100 %
F9 Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). F9 Specificity 100 % Genes 100 %
Hemophilia B. By Institute of Human Genetics Uniklinik RWTH Aachen (Germany). F9 Specificity 100 % Genes 100 %
Hemophilia B (F9) Sequencing and Deletion/Duplication. By ARUP Laboratories, Molecular Genetics and Genomics (United States). F9 Specificity 100 % Genes 100 %
Hemophilia B (F9) Deletion/Duplication. By ARUP Laboratories, Molecular Genetics and Genomics (United States). F9 Specificity 100 % Genes 100 %

You can get up to 44 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Search Engine

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