COL4A3 gene related symptoms and diseases
All the information presented here about the COL4A3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to COL4A3 gene
Symptoms // Phenotype | % Cases |
---|---|
Hearing impairment | Common - Between 50% and 80% cases |
Hypertension | Common - Between 50% and 80% cases |
Renal insufficiency | Common - Between 50% and 80% cases |
Proteinuria | Common - Between 50% and 80% cases |
Stage 5 chronic kidney disease | Common - Between 50% and 80% cases |
Other less frequent symptoms and clinical features
Patients with COL4A3 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Hematuria
- Microscopic hematuria
Not very common - Between 30% and 50% cases
- Nephritis
- Thickening of the glomerular basement membrane
- Sensorineural hearing impairment
- Diffuse glomerular basement membrane lamellation
- Myopia
- Nephrotic syndrome
And 18 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to COL4A3 gene
Here you will find a list of rare diseases related to the COL4A3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AUTOSOMAL DOMINANT ALPORT SYNDROME
Description
A genetically heterogenous disorder characterized by kidney abnormalities with hematuria and proteinuria, sensorineural hearing loss, and eye abnormalities. Two main genetically distinct forms are recognized: An X-linked dominant form (MIM 301050) with additional features including mental retardation, dysmorphic facies with midfacial hypoplasia, elliptocytosis and smooth muscle tumors; and an autosomal recessive form (OMIM 203780). Variants of Alport syndrome without mental retardation include: Alport syndrome with leukocyte inclusions and macrothrombocytopenia (transmitted as an autosomal dominant trait) Synonyms: Fechtner syndrome (named after a patient) Sebastian platelet syndrome (named after a patient) macrothrombocytopathy-deafness-nephritis-leukocyte inclusions syndrome (OMIM 153640) Alport syndrome with macrothrombocytopenia (transmitted as an autosomal dominant trait) Synonyms: Epstein syndrome hereditary macrothrombocytopathia-nephritis-deafness syndrome macrothrombocytopathy-nephritis-deafness syndrome thrombocytopenia-macrothrombocytopathia-nephritis-defames syndrome (OMIM 153650) hereditary nephropathy-deafness syndrome (transmitted as an autosomal dominant trait) Synonym: hereditary nephropathy-sensorineural hearing loss syndrome (OMIM 104200) Alport syndrome with abnormal collagen of basement membrane (transmitted as an X-linked trait) (OMIM 303630)
More info about AUTOSOMAL DOMINANT ALPORT SYNDROME
SOURCES: ORPHANET
ALPORT SYNDROME, AUTOSOMAL DOMINANT
Description
Alport syndrome classically comprises nephritis, often progressing to renal failure, and sensorineural hearing loss (Alport, 1927). For a general phenotypic description of Alport syndrome, see the X-linked dominant form (OMIM ). Approximately 85% of cases of Alport syndrome are X-linked and about 15% are autosomal recessive (OMIM ); autosomal dominant inheritance is rare (van der Loop et al., 2000).Also see benign familial hematuria (BFH ), a similar but milder disorder also caused by mutation in the COL4A3 gene.An autosomal dominant disorder sharing the clinical features of Alport syndrome but with the addition of macrothrombocytopenia, known as Fechtner syndrome (OMIM ), is caused by mutation in the MYH9 gene (OMIM ) on chromosome 22q11.
Most common symptoms of ALPORT SYNDROME, AUTOSOMAL DOMINANT
- Hearing impairment
- Sensorineural hearing impairment
- Hypertension
- Myopia
- Renal insufficiency
More info about ALPORT SYNDROME, AUTOSOMAL DOMINANT
SOURCES: OMIM
AUTOSOMAL RECESSIVE ALPORT SYNDROME
Description
Alport syndrome is a hereditary disorder of the basement membrane, resulting in a glomerulonephropathy causing renal failure. Progressive deafness and ocular anomalies may also occur (Mochizuki et al., 1994; Colville et al. (1997)). For a general phenotypic description of Alport syndrome, see the X-linked dominant form (OMIM ). Approximately 85% of cases of Alport syndrome are X-linked and about 15% are autosomal recessive; autosomal dominant inheritance (OMIM ) is rare (van der Loop et al., 2000).See also benign familial hematuria (BFH ), a similar but milder disorder.
Most common symptoms of AUTOSOMAL RECESSIVE ALPORT SYNDROME
- Hearing impairment
- Failure to thrive
- Sensorineural hearing impairment
- Cataract
- Hypertension
More info about AUTOSOMAL RECESSIVE ALPORT SYNDROME
HEMATURIA, BENIGN FAMILIAL; BFH
Alternate names
HEMATURIA, BENIGN FAMILIAL; BFH Is also known as tmn, thin membrane nephropathy, thin-basement-membrane nephropathy
Description
Benign familial hematuria is an autosomal dominant condition manifest as nonprogressive isolated microscopic hematuria that does not result in renal failure. It is characterized pathologically by thinning of the glomerular basement membrane (GBM), and can be considered the mildest end of the spectrum of renal diseases due to type IV collagen defects of the basement membrane. The most severe end of the spectrum is represented by Alport syndrome ({301050}; {203780}, {104200}), which results in end-stage renal failure and may be associated with hearing loss and ocular anomalies (review by Lemmink et al. (1996)).
Most common symptoms of HEMATURIA, BENIGN FAMILIAL; BFH
- Hearing impairment
- Hypertension
- Renal insufficiency
- Proteinuria
- Stage 5 chronic kidney disease
More info about HEMATURIA, BENIGN FAMILIAL; BFH
FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS
Alternate names
FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS Is also known as familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis
More info about FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS
SOURCES: ORPHANET
Search interest in COL4A3
Potential gene panels for COL4A3 gene
GeneAware Complete Panel Version 2 (Female) Panel
By Baylor Miraca Genetics Laboratories GeneAware Complete Panel Version 2 (Female) that also includes the following genes: RMRP BCS1L SACS BLM SGCA SGCB SGCG SGSH SLC12A6 SLC17A5
More info about this panelGeneAware Complete Panel Version 2 (Male) Panel
By Baylor Miraca Genetics Laboratories GeneAware Complete Panel Version 2 (Male) that also includes the following genes: RMRP BCS1L SACS BLM SGCA SGCB SGCG SGSH SLC12A6 SLC17A5
More info about this panelGeneAware Ashkenazi Jewish Panel Version 2 (Female) Panel
By Baylor Miraca Genetics Laboratories GeneAware Ashkenazi Jewish Panel Version 2 (Female) that also includes the following genes: BLM SLC35A3 SMN1 SMPD1 CLRN1 MCOLN1 PCDH15 RTEL1 CFTR SUMF1
More info about this panelGeneAware Ashkenazi Jewish Panel Version 2 (Male) Panel
By Baylor Miraca Genetics Laboratories GeneAware Ashkenazi Jewish Panel Version 2 (Male) that also includes the following genes: BLM SLC35A3 SMN1 SMPD1 CLRN1 MCOLN1 PCDH15 RTEL1 CFTR SUMF1
More info about this panelComplete Alport Syndrome Evaluation Panel
By Athena Diagnostics Inc Complete Alport Syndrome Evaluation that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelCOL4A3 DNA Sequencing Test Panel
By Athena Diagnostics Inc
This panel specifically test the COL4A3 gene.
More info about this panelHearing Loss Advanced Sequencing and CNV Evaluation Panel
By Athena Diagnostics Inc Hearing Loss Advanced Sequencing and CNV Evaluation that also includes the following genes: BCS1L ROR1 SALL1 SEMA3E SIX1 SIX5 SLC12A1 SLC19A2 SLC22A4 SNAI2
More info about this panelNGS Hearing Loss Panel Panel
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center NGS Hearing Loss Panel that also includes the following genes: SIX1 SNAI2 SMPX SOX10 TECTA TIMM8A TJP2 TMPRSS3 USH1C USH2A
More info about this panelAlport syndrome panel Panel
By Collagen Diagnostic Laboratory University of Washington Alport syndrome panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelOtoSCOPE Panel
By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics OtoSCOPE that also includes the following genes: ROR1 SIX1 SIX5 SLC22A4 SNAI2 SMPX SOX10 TBX1 TWNK TCOF1
More info about this panelHearing Loss Panel Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Hearing Loss Panel that also includes the following genes: RPS6KA3 SALL1 SEMA3E SIX1 SIX5 SLC19A2 SNAI2 SMPX SOX10 BTD
More info about this panelOtoGenome Test for Hearing Loss (110 Genes) Panel
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine OtoGenome Test for Hearing Loss (110 Genes) that also includes the following genes: BCS1L SIX1 SNAI2 SMPX SOX10 TECTA TIMM8A TMPRSS3 USH1C USH2A
More info about this panelExome PLUS Proteinuria/FSGS & Hematuria Panel
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine Exome PLUS Proteinuria/FSGS & Hematuria that also includes the following genes: CFB TRPC6 TSC1 TSC2 C1QA C1QC WT1 C3 NPHS2 ADAMTS13
More info about this panelCOL4A3. Complete sequencing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the COL4A3 gene.
More info about this panelCOL4A3, COL4A4, COL4A5. NextGeneDx.Complete sequencing by NGS Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica COL4A3, COL4A4, COL4A5. NextGeneDx.Complete sequencing by NGS that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelCOL4A3, COL4A4. NextGeneDx.Complete sequencing by NGS Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica COL4A3, COL4A4. NextGeneDx.Complete sequencing by NGS that also includes the following genes: COL4A3 COL4A4
More info about this panelAlport Syndrome Del/Dup Panel Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Alport Syndrome Del/Dup Panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport Syndrome Seq Analysis Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Alport Syndrome Seq Analysis that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport Syndrome Seq + Del/Dup Panel Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Alport Syndrome Seq + Del/Dup Panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAudiome (hearing loss panel) Panel
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia Audiome (hearing loss panel) that also includes the following genes: BCS1L SIX1 SNAI2 SMPX SOX10 SUCLA2 TECTA TIMM8A TMPRSS3 USH1C
More info about this panelAlport Syndrome (sequence analysis of COL4A3 gene) Panel
By CGC Genetics
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome (NGS panel for 3 genes) Panel
By CGC Genetics Alport syndrome (NGS panel for 3 genes) that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelSyndromic deafness (NGS panel for 62 genes) Panel
By CGC Genetics Syndromic deafness (NGS panel for 62 genes) that also includes the following genes: SEMA3E SIX1 SIX5 SLC19A2 SNAI2 SOX10 TCOF1 TFAP2A TIMM8A TYR
More info about this panelSyndromic and non syndromic deafness (NGS panel for 127 genes) Panel
By CGC Genetics Syndromic and non syndromic deafness (NGS panel for 127 genes) that also includes the following genes: SEMA3E SIX1 SIX5 SLC12A1 SLC19A2 SNAI2 SMPX SOX10 TCOF1 TECTA
More info about this panelAlport syndrome, autosomal dominant Panel
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome, autosomal recessive Panel
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Alport syndrome, autosomal recessive that also includes the following genes: COL4A3 COL4A4
More info about this panelAlport Syndrome Panel
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Alport Syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelNephrotic Syndrome (NS)/Focal Segmental Glomerulosclerosis (FSGS) Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Nephrotic Syndrome (NS)/Focal Segmental Glomerulosclerosis (FSGS) Sequencing Panel with CNV Detection that also includes the following genes: SGPL1 SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP TP53RK ACTN4 SCARB2
More info about this panelAlport Syndrome (AS) Sequencing Panel Panel
By PreventionGenetics PreventionGenetics Alport Syndrome (AS) Sequencing Panel that also includes the following genes: COL4A3 COL4A4 COL4A5 COL4A6
More info about this panelAlport Syndrome (AS) via COL4A3 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome Comprehensive panel Panel
By Connective Tissue Gene Tests Alport syndrome Comprehensive panel that also includes the following genes: COL4A3 COL4A4 COL4A5 COL4A6
More info about this panelAlport syndrome Deletion/ Duplication panel Panel
By Connective Tissue Gene Tests Alport syndrome Deletion/ Duplication panel that also includes the following genes: COL4A3 COL4A4 COL4A5 COL4A6
More info about this panelAlport syndrome NGS panel Panel
By Connective Tissue Gene Tests Alport syndrome NGS panel that also includes the following genes: COL4A3 COL4A4 COL4A5 COL4A6
More info about this panelNephrotic syndrome and related disorders Comprehensive panel Panel
By Connective Tissue Gene Tests Nephrotic syndrome and related disorders Comprehensive panel that also includes the following genes: SGPL1 SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 SCARB2 PLCE1
More info about this panelNephrotic syndrome and related disorders NGS panel Panel
By Connective Tissue Gene Tests Nephrotic syndrome and related disorders NGS panel that also includes the following genes: SGPL1 SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 SCARB2 PLCE1
More info about this panelNephrotic syndrome and related disorders Deletion / Duplication panel Panel
By Connective Tissue Gene Tests Nephrotic syndrome and related disorders Deletion / Duplication panel that also includes the following genes: SGPL1 SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 SCARB2 PLCE1
More info about this panelAlport syndrome Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Alport syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelHereditary kidney disorders - different panels Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Hereditary kidney disorders - different panels that also includes the following genes: BCS1L ROBO2 CNNM2 CFB SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8
More info about this panelNephrology Endocrinology and Electrolytes - panels Panel
By MGZ Medical Genetics Center Nephrology Endocrinology and Electrolytes - panels that also includes the following genes: ROBO2 SALL1 BLK BMP4 BMP7 SIX1 SIX2 SIX5 SLC12A1 SLC12A3
More info about this panelAlport syndrome Panel
By Bioscientia GmbH Center for Human Genetics Alport syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport syndrome, autosomal dominant/ autosomal recessive Panel
By Bioscientia GmbH Center for Human Genetics
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome, autosomal dominant/ autosomal recessive Panel
By Bioscientia GmbH Center for Human Genetics Alport syndrome, autosomal dominant/ autosomal recessive that also includes the following genes: COL4A3 COL4A4
More info about this panelAlport syndrome Panel
By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München Alport syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport syndrome, AR Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome, AR Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome panel Panel
By Centogene AG - the Rare Disease Company Alport syndrome panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelSyndromic Hearing Loss Panel Panel
By CeGaT GmbH Syndromic Hearing Loss Panel that also includes the following genes: SEMA3E SIX1 SIX5 SLC19A2 SNAI2 SOX10 TCOF1 TFAP2A TIMM8A TYR
More info about this panelAlport Syndrome Panel Panel
By CeGaT GmbH Alport Syndrome Panel that also includes the following genes: CD151 COL4A3 COL4A4 COL4A5 EIF2AK3 MYH9
More info about this panelSingle gene testing COL4A3 Panel
By CeGaT GmbH
This panel specifically test the COL4A3 gene.
More info about this panelAlport syndrome Panel
By Laboratory of Human Genetics GENOMED Health Care Center Alport syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport Syndrome Panel
By Asper Biogene Asper Biogene LLC Alport Syndrome that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelVitreoretinopathy panel Panel
By Molecular Vision Laboratory Vitreoretinopathy panel that also includes the following genes: ATOH7 CAPN5 ZNF408 TSPAN12 COL11A1 COL11A2 COL18A1 COL4A3 COL4A4 COL4A5
More info about this panelALPORT, SYNDROME Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases ALPORT, SYNDROME that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport syndrome: COL4A3 gene sequence analysis (DNA) Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the COL4A3 gene.
More info about this panelHearing Loss: Sequencing Panel Panel
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Hearing Loss: Sequencing Panel that also includes the following genes: RPS6KA3 SALL1 SIX1 SIX5 SMPX SOX10 BTD TCOF1 TECTA TIMM8A
More info about this panelAlport Syndrome, COL4A3-related Panel
By Integrated Genetics Westborough Integrated Genetics
This panel specifically test the COL4A3 gene.
More info about this panelInheritest NGS, Ashkenazi Jewish Ancestry Panel Panel
By Integrated Genetics Westborough Integrated Genetics Inheritest NGS, Ashkenazi Jewish Ancestry Panel that also includes the following genes: BLM SLC35A3 SMN1 SMPD1 CLRN1 MCOLN1 PCDH15 CFTR SUMF1 DHDDS
More info about this panelInheritest NGS, Comprehensive Panel
By Integrated Genetics Westborough Integrated Genetics Inheritest NGS, Comprehensive that also includes the following genes: RMRP BCS1L SACS BLM SGSH SLC12A6 SLC17A5 SLC22A5 SLC26A2 SLC35A3
More info about this panelAlport Syndrome NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Alport Syndrome NGS Panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelCOL4A3 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the COL4A3 gene.
More info about this panelKidneySeq - 264 Genes Panel
By Iowa Institute of Human Genetics University of Iowa KidneySeq - 264 Genes that also includes the following genes: ROBO2 CNNM2 SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8 BMP4 SEMA3E
More info about this panelNephrotic Syndrome Panel Panel
By Blueprint Genetics Nephrotic Syndrome Panel that also includes the following genes: SGPL1 SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 SCARB2 PLCE1
More info about this panelComprehensive Hearing Loss and Deafness Panel Panel
By Blueprint Genetics Comprehensive Hearing Loss and Deafness Panel that also includes the following genes: BCS1L RPS6KA3 SALL1 SEMA3E SIX1 SIX5 SLC19A2 SNAI2 SMPX SOX10
More info about this panelSyndromic Hearing Loss Panel Panel
By Blueprint Genetics Syndromic Hearing Loss Panel that also includes the following genes: BCS1L SALL1 SEMA3E SIX1 SIX5 SLC19A2 SNAI2 SOX10 BTD TWNK
More info about this panelAlport Syndrome Panel Panel
By Blueprint Genetics Alport Syndrome Panel that also includes the following genes: CD151 COL4A3 COL4A4 COL4A5 COL4A6 MYH9
More info about this panelAlport syndrome Panel
By Bioarray
This panel specifically test the COL4A3 gene.
More info about this panelAlport Syndrome Gene Set Panel
By Genomics and Pathology Services Washington University in St. Louis Alport Syndrome Gene Set that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelNephrotic Syndrome and Focal Segmental Glomerulosclerosis Gene Set Panel
By Genomics and Pathology Services Washington University in St. Louis Nephrotic Syndrome and Focal Segmental Glomerulosclerosis Gene Set that also includes the following genes: SMARCAL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 SCARB2 PLCE1 CRB2
More info about this panelSYNDROME WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS NGS PANEL Panel
By Laboratorio de Genetica Clinica SL SYNDROME WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS NGS PANEL that also includes the following genes: SGPL1 TRPC6 WT1 NPHS2 ANLN CD2AP ACTN4 PLCE1 NUP205 CRB2
More info about this panelBENIGN FAMILIAL HEMATURIA Panel
By Laboratorio de Genetica Clinica SL BENIGN FAMILIAL HEMATURIA that also includes the following genes: COL4A3 CFH
More info about this panelALPORT SYNDROME Panel
By Laboratorio de Genetica Clinica SL ALPORT SYNDROME that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport & Stickler syndrome hearing loss panel Panel
By LifeLabs Genetics Alport & Stickler syndrome hearing loss panel that also includes the following genes: COL11A2 COL4A3 COL4A4 COL4A5 COL9A1 COL9A2 EDNRB
More info about this panelAlport syndrome panel Panel
By LifeLabs Genetics Alport syndrome panel that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport Syndrome, Massive Sequencing (NGS) COL4A5 , COL4A3, COL4A4 Genes Panel
By Reference Laboratory Genetics Alport Syndrome, Massive Sequencing (NGS) COL4A5 , COL4A3, COL4A4 Genes that also includes the following genes: COL4A3 COL4A4 COL4A5
More info about this panelAlport Syndrome , Deletions-Duplications (MLPA) COL4A3 Gene Panel
By Reference Laboratory Genetics
This panel specifically test the COL4A3 gene.
More info about this panelAlport Syndrome, Sequencing COL4A3 Gene Panel
By Reference Laboratory Genetics
This panel specifically test the COL4A3 gene.
More info about this panelBenign Familial Hematuria , Sequencing COL4A3 Gene Panel
By Reference Laboratory Genetics
This panel specifically test the COL4A3 gene.
More info about this panelBenign Familial Hematuria, Massive Sequencing COL4A3, COL4A4 Genes Panel
By Reference Laboratory Genetics Benign Familial Hematuria, Massive Sequencing COL4A3, COL4A4 Genes that also includes the following genes: COL4A3 COL4A4
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