MAPT gene related symptoms and diseases
All the information presented here about the MAPT gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to MAPT gene
Symptoms // Phenotype | % Cases |
---|---|
Dementia | Common - Between 50% and 80% cases |
Frontotemporal dementia | Common - Between 50% and 80% cases |
Mental deterioration | Common - Between 50% and 80% cases |
Behavioral abnormality | Common - Between 50% and 80% cases |
Personality changes | Common - Between 50% and 80% cases |
Other less frequent symptoms and clinical features
Patients with MAPT gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Parkinsonism
- Neurofibrillary tangles
- Aphasia
- Alzheimer disease
- Rigidity
Not very common - Between 30% and 50% cases
- Neuronal loss in central nervous system
- Hyperreflexia
- Postural instability
And 143 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to MAPT gene
Here you will find a list of rare diseases related to the MAPT. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
PICK DISEASE OF BRAIN
Alternate names
PICK DISEASE OF BRAIN Is also known as dementia with lobar atrophy and neuronal cytoplasmic inclusions, lobar atrophy of brain
Description
Pick disease refers to the neuropathologic finding of 'Pick bodies,' which are argyrophilic, intraneuronal inclusions, and 'Pick cells,' which are enlarged neurons. The clinical correlates of Pick disease of brain include those of frontotemporal dementia, which encompass the behavioral variant of FTD, semantic dementia, and progressive nonfluent aphasia (summary by Piguet et al., 2011).Kertesz (2003) suggested the term 'Pick complex' to represent the overlapping syndromes of FTD, primary progressive aphasia (PPA), corticobasal degeneration (CBD), progressive supranuclear palsy (OMIM ), and FTD with motor neuron disease. He noted that frontotemporal dementia may also be referred to as 'clinical Pick disease,' and that the term 'Pick disease' should be restricted to the pathologic finding of Pick bodies.
Most common symptoms of PICK DISEASE OF BRAIN
- Ventriculomegaly
- Behavioral abnormality
- Dementia
- Cerebral cortical atrophy
- Rigidity
PARKINSON-DEMENTIA SYNDROME
Most common symptoms of PARKINSON-DEMENTIA SYNDROME
- Hyperreflexia
- Dysarthria
- Tremor
- Dementia
- Kyphoscoliosis
CLASSIC PROGRESSIVE SUPRANUCLEAR PALSY SYNDROME
Alternate names
CLASSIC PROGRESSIVE SUPRANUCLEAR PALSY SYNDROME Is also known as psp, steele-richardson-olszewski disease, steele-richardson-olszewski syndrome, classic psp syndrome, richardson syndrome
Description
Classical progressive supranuclear palsy, also known as Richardson's syndrome, is the most common clinical variant of progressive supranuclear palsy (PSP; see this term), a rare late-onset neurodegenerative disease characterized by postural instability, progressive rigidity, supranuclear gaze palsy and mild dementia.
Most common symptoms of CLASSIC PROGRESSIVE SUPRANUCLEAR PALSY SYNDROME
- Seizures
- Cognitive impairment
- Hyperreflexia
- Dysarthria
- Tremor
FRONTOTEMPORAL DEMENTIA; FTD
Alternate names
FRONTOTEMPORAL DEMENTIA; FTD Is also known as mstd, frontotemporal dementia with parkinsonism, ftld with tau inclusions, ddpac, ftdp17, wilhelmsen-lynch disease, pallidopontonigral degeneration, frontotemporal lobar degeneration with tau inclusions, frontotemporal lobe dementia, disinhibition-dementia-parkins
Description
Frontotemporal dementia (FTD) refers to a clinical manifestation of the pathologic finding of frontotemporal lobar degeneration (FTLD). FTD, the most common subtype of FTLD, is a behavioral variant characterized by changes in social and personal conduct with loss of volition, executive dysfunction, loss of abstract thought, and decreased speech output. A second clinical subtype of FTLD is 'semantic dementia,' characterized by specific loss of comprehension of language and impaired facial and object recognition. A third clinical subtype of FTLD is 'primary progressive aphasia' (PPA), characterized by a reduction in speech production, speech errors, and word retrieval difficulties resulting in mutism and an inability to communicate. All subtypes have relative preservation of memory, at least in the early stages. FTLD is often associated with parkinsonism or motor neuron disease (MND) resembling amyotrophic lateral sclerosis (ALS ) (reviews by Tolnay and Probst, 2002 and Mackenzie and Rademakers, 2007). {30,31:Mackenzie et al. (2009, 2010)} provided a classification of FTLD subtypes according to the neuropathologic findings (see PATHOGENESIS below).
Most common symptoms of FRONTOTEMPORAL DEMENTIA; FTD
- Hyperreflexia
- Dysarthria
- Skeletal muscle atrophy
- Tremor
- Dysphagia
PARKINSON DISEASE, LATE-ONSET; PD
Alternate names
PARKINSON DISEASE, LATE-ONSET; PD Is also known as park
Description
Parkinson disease was first described by James Parkinson in 1817. It is the second most common neurodegenerative disorder after Alzheimer disease (AD ), affecting approximately 1% of the population over age 50 (Polymeropoulos et al., 1996).
Most common symptoms of PARKINSON DISEASE, LATE-ONSET; PD
- Ataxia
- Cognitive impairment
- Dysarthria
- Tremor
- Dysphagia
SOURCES: OMIM
SEMANTIC DEMENTIA
Alternate names
SEMANTIC DEMENTIA Is also known as semantic primary progressive aphasia, semantic variant ppa
Description
Semantic dementia (SD) is a form of frontotemporal dementia (FTD; see this term), characterized by the progressive, amodal and profound loss of semantic knowledge (combination of visual associative agnosia, anomia, surface dyslexia or dysgraphia and disrupted comprehension of word meaning) and behavioral abnormalities, attributable to the degeneration of the anterior temporal lobes.
Most common symptoms of SEMANTIC DEMENTIA
- Dementia
- Neurological speech impairment
- Brain atrophy
- Aphasia
- Dyslexia
SOURCES: ORPHANET
PROGRESSIVE NON-FLUENT APHASIA
Alternate names
PROGRESSIVE NON-FLUENT APHASIA Is also known as agramatic variant of primary progressive aphasia, agramatic variant of ppa, non-fluent variant ppa
Description
Progressive non-fluent aphasia (PNFA) is a form of frontotemporal dementia (FTD; see this term), characterized by agrammatism, laborious speech, alexia, and agraphia, frequently accompanied by apraxia of speech (AOS). Language comprehension is relatively preserved.
Most common symptoms of PROGRESSIVE NON-FLUENT APHASIA
- Behavioral abnormality
- Depressivity
- Anxiety
- Mental deterioration
- Stroke
SOURCES: ORPHANET
BEHAVIORAL VARIANT OF FRONTOTEMPORAL DEMENTIA
Alternate names
BEHAVIORAL VARIANT OF FRONTOTEMPORAL DEMENTIA Is also known as bv-ftd
Description
Behavioral variant of frontotemporal dementia (bv-FTD) is a form of frontotemporal dementia (FTD; see this term), characterized by progressive behavioral impairment and a decline in executive function with frontal lobe-predominant atrophy.
Most common symptoms of BEHAVIORAL VARIANT OF FRONTOTEMPORAL DEMENTIA
- Hyperreflexia
- Gait disturbance
- Behavioral abnormality
- Aggressive behavior
- Mental deterioration
SOURCES: ORPHANET
Search interest in MAPT
Potential gene panels for MAPT gene
MAPT DNA Sequencing Test Panel
By Athena Diagnostics Inc
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Dementia (FTD) Evaluation Panel
By Athena Diagnostics Inc Frontotemporal Dementia (FTD) Evaluation that also includes the following genes: C9orf72 GRN MAPT
More info about this panelFrontotemporal Dementia (FTDP) - MAPT Gene, Exon 10 Only Panel
By Center for Genetics at Saint Francis Saint Francis Hospital
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Dementia w/ Parkinsonism (FTDP) - MAPT Gene Panel
By Center for Genetics at Saint Francis Saint Francis Hospital
This panel specifically test the MAPT gene.
More info about this panelDementia Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Dementia that also includes the following genes: SORL1 TARDBP VCP FIG4 OPTN TREM2 CSF1R CHMP2B DCTN1 C9orf72
More info about this panelMovement Disorders Panel Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Movement Disorders Panel that also includes the following genes: SCP2 SGCE SLC20A2 SLC2A1 SLC6A3 SNCA SPR SQSTM1 SUCLA2 SUOX
More info about this panelParkinson's Disease Panel
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Parkinson's Disease that also includes the following genes: SLC6A3 SNCA TAF1 TH VPS35 FBXO7 PINK1 PARK7 LRRK2 CSF1R
More info about this panelMAPT. Complete sequencing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the MAPT gene.
More info about this panelGRN, MAPT. MLPA testing (exons 1,3,6,10 and 12 gene GRN and exons 2 to 13 gene MAPT) Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica GRN, MAPT. MLPA testing (exons 1,3,6,10 and 12 gene GRN and exons 2 to 13 gene MAPT) that also includes the following genes: GRN MAPT
More info about this panelMAPT. Complete sequencing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the MAPT gene.
More info about this panelMAPT. Sequencing of the exons 1, 9, 10, 11, 12 and 13 Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the MAPT gene.
More info about this panelMAPT. Sequencing of the exons 1, 9, 10, 11, 12 and 13 Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the MAPT gene.
More info about this panelMAPT, GRN. MLPA testing Panel
By Instituto de Medicina Genomica Instituto de Medicina Genomica MAPT, GRN. MLPA testing that also includes the following genes: GRN MAPT
More info about this panelFrontotemporal Dementia (sequence analysis of MAPT gene) Panel
By CGC Genetics
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal dementia (NGS panel for 13 genes) Panel
By CGC Genetics Frontotemporal dementia (NGS panel for 13 genes) that also includes the following genes: TARDBP TUBA4A UBQLN2 VCP CHCHD10 CSF1R CHMP2B FUS GRN HNRNPA1
More info about this panelParkinson disease (NGS panel for 33 genes) Panel
By CGC Genetics Parkinson disease (NGS panel for 33 genes) that also includes the following genes: SLC6A3 SNCA SNCAIP SNCB SYNJ1 TAF1 TH GIGYF2 UCHL1 VPS35
More info about this panelHereditary dementias (NGS panel for 28 genes) Panel
By CGC Genetics Hereditary dementias (NGS panel for 28 genes) that also includes the following genes: SNCA SNCB SORL1 TARDBP TIMM8A TUBA4A TYROBP UBQLN2 VCP CHCHD10
More info about this panelAmyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection that also includes the following genes: SOD1 SQSTM1 TARDBP TBK1 UBQLN2 VAPB VCP OPTN CDH13 TREM2
More info about this panelFrontotemporal Dementia via MAPT Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the MAPT gene.
More info about this panelParkinson Disease Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Parkinson Disease Sequencing Panel with CNV Detection that also includes the following genes: SLC6A3 SNCA SPR SYNJ1 TAF1 GIGYF2 UCHL1 VPS35 FBXO7 HTRA2
More info about this panelDementia Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Dementia Sequencing Panel with CNV Detection that also includes the following genes: SQSTM1 TARDBP TYROBP UBQLN2 TREM2 CHMP2B C9orf72 FUS GRN APP
More info about this panelParkinson Disease and Parkinsonism Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Parkinson Disease and Parkinsonism Sequencing Panel with CNV Detection that also includes the following genes: SLC20A2 SLC6A3 SNCA SNCB SPG11 SPR SYNJ1 TAF1 TARDBP TWNK
More info about this panelNeurogenetic Disorders - panels Panel
By MGZ Medical Genetics Center Neurogenetic Disorders - panels that also includes the following genes: BCS1L RTN2 RYR1 SACS SCN1A SCN1B SCN2A SCN8A SCO1 SCO2
More info about this panelFTD - ALS panel Panel
By Genome Diagnostics Laboratory University Medical Center Utrecht FTD - ALS panel that also includes the following genes: SMPD1 SOD1 TARDBP VAPB VCP NPC2 FIG4 CHMP2B FUS ALS2
More info about this panelAllNeuro panel Panel
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panelDementia, frontotemporal Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the MAPT gene.
More info about this panelParkinsons disease panel Panel
By Centogene AG - the Rare Disease Company Parkinsons disease panel that also includes the following genes: SLC6A3 SNCA SNCB SPR SYNJ1 TAF1 TH GIGYF2 UCHL1 VPS35
More info about this panelAmyotrophic Lateral Sclerosis NGS Panel + C9orf72 Repeat Expansion Panel
By MNG Laboratories (Medical Neurogenetics, LLC.) Amyotrophic Lateral Sclerosis NGS Panel + C9orf72 Repeat Expansion that also includes the following genes: SOD1 SPG11 SQSTM1 TARDBP UBQLN2 VAPB VCP PARK7 FIG4 OPTN
More info about this panelAmyotrophic Lateral Sclerosis NGS Panel Panel
By MNG Laboratories (Medical Neurogenetics, LLC.) Amyotrophic Lateral Sclerosis NGS Panel that also includes the following genes: SOD1 SPG11 SQSTM1 TARDBP UBQLN2 VAPB VCP PARK7 FIG4 OPTN
More info about this panelAmyotrophic Lateral Sclerosis (ALS) Panel Panel
By CeGaT GmbH Amyotrophic Lateral Sclerosis (ALS) Panel that also includes the following genes: ATXN1 ATXN2 SOD1 SPG11 SQSTM1 TAF15 TARDBP TBK1 TUBA4A UBQLN2
More info about this panelParkinson all Panel Panel
By CeGaT GmbH Parkinson all Panel that also includes the following genes: ATXN2 SLC6A3 SNCA SPG11 SPR SYNJ1 TAF1 TH VPS35 FBXO7
More info about this panelFrontotemporal Dementia (FTD) Panel Panel
By CeGaT GmbH Frontotemporal Dementia (FTD) Panel that also includes the following genes: ATXN2 SQSTM1 TARDBP TBK1 TUBA4A UBQLN2 VCP CHCHD10 OPTN TREM2
More info about this panelAtypical Parkinson syndrome Panel Panel
By CeGaT GmbH Atypical Parkinson syndrome Panel that also includes the following genes: ATXN2 SPG11 SYNJ1 TH FBXO7 DNAJC6 RAB39B ATP6AP2 ZFYVE26 SLC30A10
More info about this panelDementia all Panel Panel
By CeGaT GmbH Dementia all Panel that also includes the following genes: ATXN2 SQSTM1 TARDBP TBK1 TBP TUBA4A UBQLN2 VCP VPS35 MARK4
More info about this panelSingle gene testing MAPT Panel
By CeGaT GmbH
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Dementia (MAPT and GRN) Panel
By MVZ Dortmund Dr. Eberhard & Partner Frontotemporal Dementia (MAPT and GRN) that also includes the following genes: GRN MAPT
More info about this panelFrontotemporal Dementia Panel
By Asper Biogene Asper Biogene LLC Frontotemporal Dementia that also includes the following genes: TARDBP CHMP2B GRN MAPT
More info about this panelParkinson Disease Panel
By Asper Biogene Asper Biogene LLC Parkinson Disease that also includes the following genes: SLC6A3 SNCA SPR SYNJ1 TAF1 TH GIGYF2 UCHL1 VPS35 FBXO7
More info about this panelFrontotemporal dementia, MAPT sequencing Panel
By Molecular Diagnostics Laboratory University of Toledo Medical Center
This panel specifically test the MAPT gene.
More info about this panelTest for MAPT-Related Disorders Panel
By Secugen SL
This panel specifically test the MAPT gene.
More info about this panelDementia, frontotemporal, with or without parkinsonism Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the MAPT gene.
More info about this panelPick disease Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the MAPT gene.
More info about this panelSupranuclear palsy, progressive Panel
By Praxis fuer Humangenetik Wien
This panel specifically test the MAPT gene.
More info about this panelqChip Panel
By Quantitative Genomic Medicine Laboratories, SL qChip that also includes the following genes: RS1 RUNX2 SALL1 SCN1A BMPR1A SH2D1A SEM1 SHH SHOX SIM1
More info about this panelDementia, frontotemporal, with or without parkinsonism Panel
By MedGene
This panel specifically test the MAPT gene.
More info about this panelPick disease Panel
By MedGene
This panel specifically test the MAPT gene.
More info about this panelSupranuclear palsy, progressive Panel
By MedGene
This panel specifically test the MAPT gene.
More info about this panelInvitae Combined Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel Panel
By Invitae Invitae Combined Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel that also includes the following genes: SNCA SOD1 SPG11 TARDBP TBK1 TFG UBQLN2 VAPB VCP CHCHD10
More info about this panelInvitae Frontotemporal Dementia Panel Panel
By Invitae Invitae Frontotemporal Dementia Panel that also includes the following genes: TARDBP TBK1 UBQLN2 VCP CHCHD10 DCTN1 FUS GRN MAPT
More info about this panelAlzheimer: Apo-E, PSEN1, PSEN2, APP, A2M and MAPT genes sequence analysis (select exons) Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Alzheimer: Apo-E, PSEN1, PSEN2, APP, A2M and MAPT genes sequence analysis (select exons) that also includes the following genes: APOE APP MAPT A2M PSEN1 PSEN2
More info about this panelAlzheimer: MAPT, CLU, PICALM, CR1 genes screening Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Alzheimer: MAPT, CLU, PICALM, CR1 genes screening that also includes the following genes: PICALM CLU CR1 MAPT
More info about this panelFrontotemporal dementia: MAPT and PGRN genes deletions-duplications analysis (MLPA) Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Frontotemporal dementia: MAPT and PGRN genes deletions-duplications analysis (MLPA) that also includes the following genes: GRN MAPT
More info about this panelFrontotemporal dementia: MAPT gene sequence analysis Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal dementia Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Frontotemporal dementia that also includes the following genes: TARDBP UBQLN2 VCP CHMP2B FUS GRN MAPT SIGMAR1
More info about this panelNGS panel - dementia Panel
By Genome Diagnostics VU University Medical Center NGS panel - dementia that also includes the following genes: SNCA SNCB SOD1 SORL1 SQSTM1 TARDBP TYROBP UBAP1 UBQLN2 VAPB
More info about this panelNGS panel - Parkinson Panel
By Genome Diagnostics VU University Medical Center NGS panel - Parkinson that also includes the following genes: ATXN2 SLC18A2 SLC6A3 SNCA SPR SYNJ1 TAF1 TH GIGYF2 UCHL1
More info about this panelMAPT - Gene sequencing Panel
By Genome Diagnostics VU University Medical Center
This panel specifically test the MAPT gene.
More info about this panelIntellectual Disability NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Intellectual Disability NGS Panel that also includes the following genes: BCS1L RPS6KA3 SACS BIN1 SCN1A SCN8A SDCCAG8 SGCA SGSH ST3GAL3
More info about this panelParkinson-Alzheimer-Dementia NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Parkinson-Alzheimer-Dementia NGS Panel that also includes the following genes: SLC6A3 SNCA SNCB TAF1 TH TYROBP UCHL1 VPS35 FBXO7 AAAS
More info about this panelMAPT Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the MAPT gene.
More info about this panelDementia Panel Panel
By Blueprint Genetics Dementia Panel that also includes the following genes: SNCA SORL1 TARDBP TUBA4A UBE3A UBQLN2 VCP TREM2 RNF216 CSF1R
More info about this panelParkinson Disease Panel Panel
By Blueprint Genetics Parkinson Disease Panel that also includes the following genes: SLC20A2 SLC6A3 SNCA SPR SYNJ1 TH VPS35 FBXO7 PINK1 DNAJC6
More info about this panelFrontotemporal dementia Panel
By Bioarray
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Lobar Degeneration (MAPT gene) Panel
By Diagnostic Service Facility University of Antwerp
This panel specifically test the MAPT gene.
More info about this panelFamilial Alzheimer Dementia (MAPT gene) Panel
By Diagnostic Service Facility University of Antwerp
This panel specifically test the MAPT gene.
More info about this panelPROGRESSIVE SUPRANUCLEAR PALSY Panel
By Laboratorio de Genetica Clinica SL
This panel specifically test the MAPT gene.
More info about this panelPICK DISEASE OF BRAIN Panel
By Laboratorio de Genetica Clinica SL
This panel specifically test the MAPT gene.
More info about this panelDEMENTIA & ALZHEIMER: NGS PANEL Panel
By Laboratorio de Genetica Clinica SL DEMENTIA & ALZHEIMER: NGS PANEL that also includes the following genes: SORL1 TARDBP VCP TREM2 CSF1R CHMP2B FUS GRN APOE ITM2B
More info about this panelFRONTOTEMPORAL DEMENTIA Panel
By Laboratorio de Genetica Clinica SL FRONTOTEMPORAL DEMENTIA that also includes the following genes: TARDBP CHMP2B C9orf72 GRN MAPT PSEN1
More info about this panelClassic Progressive Supranuclear Palsy , Sequencing MAPT Gene Panel
By Reference Laboratory Genetics
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Dementia , Sequencing MAPT Gene Panel
By Reference Laboratory Genetics
This panel specifically test the MAPT gene.
More info about this panelFrontotemporal Dementia with or without Parkinsonism , Deletions-Duplications (MLPA) MAPT Gene Panel
By Reference Laboratory Genetics
This panel specifically test the MAPT gene.
More info about this panelAlzheimer Disease, Panel Massive Sequencing (NGS) 8 Genes Panel
By Reference Laboratory Genetics Alzheimer Disease, Panel Massive Sequencing (NGS) 8 Genes that also includes the following genes: C9orf72 GRN APOE APP MAPT A2M PSEN1 PSEN2
More info about this panelFrontotemporal Dementia , Panel Massive Sequencing (NGS) 8 Genes Panel
By Reference Laboratory Genetics Frontotemporal Dementia , Panel Massive Sequencing (NGS) 8 Genes that also includes the following genes: TARDBP UBQLN2 VCP CHMP2B FUS GRN MAPT SIGMAR1
More info about this panelFrontotemporal dementia Panel
By Labor Dr. Wisplinghoff
This panel specifically test the MAPT gene.
More info about this panelMAPT-Related Disorders: gene sequencing Panel
By CEN4GEN Institute for Genomics and Molecular Diagnostics
This panel specifically test the MAPT gene.
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