SUGCT gene related symptoms and diseases

All the information presented here about the SUGCT gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to SUGCT gene

Symptoms // Phenotype % Cases
Failure to thrive Very Common - Between 80% and 100% cases
Hypertension Very Common - Between 80% and 100% cases
Vomiting Very Common - Between 80% and 100% cases
Diarrhea Very Common - Between 80% and 100% cases
Acidosis Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with SUGCT gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Aciduria
  • Goiter
  • Abnormality of mitochondrial metabolism
  • Hyperthyroidism
  • Glutaric aciduria
  • Glutaric acidemia
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Rare diseases associated to SUGCT gene

Here you will find a list of rare diseases related to the SUGCT. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


GLUTARIC ACIDEMIA TYPE 3


Alternate names

GLUTARIC ACIDEMIA TYPE 3 Is also known as glutaryl-coa oxidase deficiency, ga iii, glutaric aciduria type 3

Description

Glutaryl-CoA oxidase deficiency is a peroxisomal disorder leading to glutaric aciduria. The prevalence is unknown. There is no distinctive phenotype associated with this disorder and one of the reported cases was asymptomatic. Transmission appears to be autosomal recessive.

Most common symptoms of GLUTARIC ACIDEMIA TYPE 3

  • Failure to thrive
  • Hypertension
  • Vomiting
  • Diarrhea
  • Acidosis


More info about GLUTARIC ACIDEMIA TYPE 3

SOURCES: OMIM ORPHANET MESH


Potential gene panels for SUGCT gene

C7orf10 Deletion/Duplication Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories

This panel specifically test the SUGCT gene.

More info about this panel

C7orf10 Familial Mutation/Variant Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories

This panel specifically test the SUGCT gene.

More info about this panel

C7orf10 Prenatal Sequence Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories

This panel specifically test the SUGCT gene.

More info about this panel

C7orf10 Sequence Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories

This panel specifically test the SUGCT gene.

More info about this panel

C7orf10 Sequence and Deletion/Duplication Analysis Panel

United States.

By Baylor Miraca Genetics Laboratories

This panel specifically test the SUGCT gene.

More info about this panel

Glutaric Acidemia, Type 3 - C7ORF10 Sequencing Panel

United States.

By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado

This panel specifically test the SUGCT gene.

More info about this panel

Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel

Portugal.

By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1

More info about this panel

Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel

Portugal.

By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1

More info about this panel

CentoICU platinum plus Panel

Germany.

By Centogene AG - the Rare Disease Company CentoICU platinum plus that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC

More info about this panel

New Born testing (CentoICU) Panel

Germany.

By Centogene AG - the Rare Disease Company New Born testing (CentoICU) that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC

More info about this panel

Glutaric aciduria type 3 Panel

Germany.

By Centogene AG - the Rare Disease Company

This panel specifically test the SUGCT gene.

More info about this panel

C7orf10 Panel

Austria.

By Division Human Genetics Medical University Innsbruck

This panel specifically test the SUGCT gene.

More info about this panel

Nuclear-Mito NGS Panel Panel

United States.

By Fulgent Genetics Fulgent Genetics Nuclear-Mito NGS Panel that also includes the following genes: RNASEL BCS1L RPL35A MRPL3 RYR1 RYR2 SACS ACSM3 SARDH ATXN7

More info about this panel

SUGCT Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the SUGCT gene.

More info about this panel

Organic Acidemia/Aciduria & Cobalamin Deficiency Panel Panel

Finland.

By Blueprint Genetics Organic Acidemia/Aciduria & Cobalamin Deficiency Panel that also includes the following genes: BCS1L SLC25A1 SUCLG1 TCN2 UMPS AMN CBS SUGCT CD320 MCEE

More info about this panel

Comprehensive Metabolism Panel Panel

Finland.

By Blueprint Genetics Comprehensive Metabolism Panel that also includes the following genes: BCS1L CNNM2 RYR1 CNNM4 SCN4A SEC23B SGSH SI SLC40A1 SLC12A3

More info about this panel

Peroxisomal Disorders Panel Panel

Finland.

By Blueprint Genetics Peroxisomal Disorders Panel that also includes the following genes: ACOX1 SUGCT DYM PEX26 EBP AGPS AGXT GNPAT AMACR HSD17B4

More info about this panel

GLUTARIC ACIDURIA NGS PANEL Panel

Spain.

By Laboratorio de Genetica Clinica SL GLUTARIC ACIDURIA NGS PANEL that also includes the following genes: SUGCT ETFA ETFB ETFDH GCDH

More info about this panel


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