VEGFC gene related symptoms and diseases
All the information presented here about the VEGFC gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to VEGFC gene
Symptoms // Phenotype | % Cases |
---|---|
Hyperkeratosis | Uncommon - Between 30% and 50% cases |
Lymphedema | Uncommon - Between 30% and 50% cases |
Cellulitis | Uncommon - Between 30% and 50% cases |
Hydrocele testis | Uncommon - Between 30% and 50% cases |
Prominent superficial veins | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with VEGFC gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Toenail dysplasia
Rare diseases associated to VEGFC gene
Here you will find a list of rare diseases related to the VEGFC. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
LYMPHEDEMA, HEREDITARY, ID; LMPH1D
Most common symptoms of LYMPHEDEMA, HEREDITARY, ID; LMPH1D
- Hyperkeratosis
- Lymphedema
- Cellulitis
- Hydrocele testis
- Prominent superficial veins
More info about LYMPHEDEMA, HEREDITARY, ID; LMPH1D
SOURCES: OMIM
MILROY DISEASE
Alternate names
MILROY DISEASE Is also known as hereditary lymphedema type i, nonne-milroy lymphedema, congenital primary lymphedema
Description
Milroy disease is a frequent form of primary lymphedema (see this term) characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period.
More info about MILROY DISEASE
SOURCES: ORPHANET
Search interest in VEGFC
Potential gene panels for VEGFC gene
NGS Vascular Disorders Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center NGS Vascular Disorders Panel that also includes the following genes: SOX18 TEK VEGFC GLMN KRIT1 STAMBP GJC2 ACVRL1 CCM2 CCBE1
More info about this panelLymphedema NGS Multi-Gene Panel (36 Genes) Panel
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam Lymphedema NGS Multi-Gene Panel (36 Genes) that also includes the following genes: BRAF SOS1 SOX18 VEGFC CBL SHOC2 GJC2 TUBGCP6 CDK19 SPRED1
More info about this panelLymphedema hereditary, IA (sequence analysis of VEGFC gene) Panel
By CGC Genetics
This panel specifically test the VEGFC gene.
More info about this panelLymphedema Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Lymphedema Sequencing Panel with CNV Detection that also includes the following genes: SOX18 VEGFC GJC2 FAT4 PIEZO1 CCBE1 FLT4 FOXC2 GATA2 GJA1
More info about this panelVascular and lymphatic disorders Panel Panel
By CeGaT GmbH Vascular and lymphatic disorders Panel that also includes the following genes: SOX18 TREX1 SERPING1 VEGFC KRIT1 GJC2 ACVRL1 CCM2 FAT4 CCBE1
More info about this panelPrimary lymphedema and Hydrops fetalis Panel
By Center for Human Genetics Cliniques Universitaires Saint Luc Primary lymphedema and Hydrops fetalis that also includes the following genes: SOS1 SOX18 VEGFC GJC2 FAT4 PIEZO1 CCBE1 EPHB4 FLT4 FOXC2
More info about this panelVEGFC Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the VEGFC gene.
More info about this panelMILROY SYNDROME SANGER PANEL Panel
By Laboratorio de Genetica Clinica SL MILROY SYNDROME SANGER PANEL that also includes the following genes: VEGFC GJC2 FLT4
More info about this panelLymphedema-Lethal Restrictive Dermopathy , Panel Massive Sequencing (NGS) 7 Genes Panel
By Reference Laboratory Genetics Lymphedema-Lethal Restrictive Dermopathy , Panel Massive Sequencing (NGS) 7 Genes that also includes the following genes: SOX18 VEGFC ZMPSTE24 FLT4 FOXC2 GATA2 KIF11
More info about this panelTempus xO assay Panel
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
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