Amyloidosis, Familial Visceral

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 Amyloidosis, Familial Visceral

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Amyloidosis, Familial Visceral

Hearing impairment
Neoplasm
Pain
Hypertension
Peripheral neuropathy
Hepatomegaly
Fever
Cardiomyopathy
Edema
Splenomegaly

And another 21 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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.

Alternative names

Amyloidosis, Familial Visceral Is also known as german type amyloidosis, amyloidosis, systemic nonneuropathic, amyloidosis viii, amyloidosis, familial renal, ostertag type amyloidosis.

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.

Amyloidosis, Familial Visceral Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Platelet Disorders. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3 , (...) View the complete list with 34 more genes Panel complete gene list RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3, ANO6, ADRA2A, DHCR24, ANKRD26, MLPH, DPAGT1, NBEAL2, F8, FGA, FGB, FGG, FLNA, GATA1, GFI1B, GGCX, GNAQ, GNAS, GP1BA, HOXA11, HPS1, AP3B1, ITGA2, ITGA2B, ITGB3, KLKB1, A2M, MPL, MYH9, MYO5A, P2RX1, BLOC1S6, PLA2G7, PLAU, RAB27A Specificity 2 % Genes 34 %
FGA Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FGA Specificity 100 % Genes 34 %
FGA Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). FGA Specificity 100 % Genes 34 %
Congenital fibrinogen deficiency. By Institute of Human Genetics Uniklinik RWTH Aachen (Germany). FGA, FGB, FGG Specificity 34 % Genes 34 %
Amyloidosis caused by mutattion of fibrinogen A? chain. By Clinic of Pediatrics and Adolescent Medicine General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague (Czech Republic). FGA Specificity 100 % Genes 34 %
FGA. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). FGA Specificity 100 % Genes 34 %
Amyloidosis, hereditary renal (sequence analysis of FGA gene). By CGC Genetics (Portugal). FGA Specificity 100 % Genes 34 %
Afibrinogenemia, congenital (sequence analysis of FGA gene). By CGC Genetics (Portugal). FGA Specificity 100 % Genes 34 %

You can get up to 58 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEPHROTIC SYNDROME, TYPE 4; NPHS4 NEURALGIC AMYOTROPHY EPISODIC ATAXIA, TYPE 1; EA1 HYPOTONIA-CYSTINURIA SYNDROME BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD BARAITSER-WINTER CEREBROFRONTOFACIAL SYNDROME JERVELL AND LANGE-NIELSEN SYNDROME 1; JLNS1