DEAFNESS, AUTOSOMAL RECESSIVE 111
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
DEAFNESS, AUTOSOMAL RECESSIVE 111
|
0.400 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.
|
29961571 |
2018 |
Adenocarcinoma of lung (disorder)
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
|
28604730 |
2017 |
Carcinoma of lung
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
|
28604730 |
2017 |
Progressive sensorineural hearing impairment
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
The shape and function of thyroid were confirmed to be normal by thyroid ultrasound scan and thyroid hormone assays in 19 of the 20 patients with EVA or other inner ear malformation except one who had cystoid change in the right side of thyroid.No Pendred syndrome was diagnosed.
|
19040761 |
2008 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
Besides clinical and radiological assessments, molecular and functional studies are essential for the correct diagnosis of Pendred syndrome and non-syndromic EVA.
|
22116360 |
2011 |
Pendred's syndrome
|
0.050 |
GeneticVariation
|
disease |
BEFREE |
Loss or reduction in the function of pendrin results in both syndromic (Pendred syndrome) and non-syndromic (non-syndromic enlarged vestibular aqueduct (ns-EVA)) hearing loss.
|
22116359 |
2011 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
Nineteen patients with PS and 23 patients with nonsyndromic EVA, aged 5-53 years, were included.
|
24224479 |
2014 |
Pendred's syndrome
|
0.050 |
Biomarker
|
disease |
BEFREE |
These mutations may be of value for the diagnosis of Pendred syndrome and NSRD with EVA.
|
16924389 |
2006 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
We thus present MPZL2 as a novel gene associated with sensorineural hearing loss.
|
29982980 |
2018 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
<b>Material and Methods:</b> HRCT scanning of the temporal bones of 82 cases with normal inner ear structures and 104 cases with an EVA and bilaterally sensorineural hearing loss (SNHL) was performed.
|
31124731 |
2019 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
SLC26A4 mutations have also been identified in patients exhibiting isolated sensorineural hearing loss without apparent thyroid abnormality (nonsyndromic enlargement of the vestibular aqueduct; nonsyndromic EVA).
|
24224479 |
2014 |
Sensorineural Hearing Loss (disorder)
|
0.040 |
Biomarker
|
disease |
BEFREE |
A total of 271 children with nonsyndromic sensorineural hearing loss and EVA underwent SLC26A4 gene screening.
|
24245694 |
2013 |
Carotid Stenosis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Follow-up data from 2184 carotid artery stenting and 2261 carotid endarterectomy patients from 4 randomized trials (EVA-3S [Endarterectomy Versus Angioplasty in Patients With Symptomatic Severe Carotid Stenosis], SPACE [Stent-Protected Angioplasty Versus Carotid Endarterectomy], ICSS [International Carotid Stenting Study], and CREST [Carotid Revascularization Endarterectomy Versus Stenting Trial]) were used to validate 23 short-term outcome models to estimate stroke or death risk ≤30 days after the procedure and the original outcome measure for which the model was developed.
|
30012816 |
2018 |
Carotid Stenosis
|
0.020 |
Biomarker
|
disease |
BEFREE |
Methods- We combined individual patient data of 4754 patients with symptomatic carotid stenosis from 4 randomized trials (EVA-3S [Endarterectomy Versus Angioplasty in Patients With Symptomatic Severe Carotid Stenosis], SPACE [Stent-Protected Angioplasty Versus Carotid Endarterectomy], ICSS [International Carotid Stenting Study], and CREST [Carotid Revascularization Endarterectomy Versus Stenting Trial]).
|
30621529 |
2019 |
Paraganglioma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
The value of a rapid contrast-enhanced angio-MRI protocol in the detection of head and neck paragangliomas in SDHx mutations carriers: a retrospective study on behalf of the PGL.EVA investigators.
|
26427697 |
2016 |
Paraganglioma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.
|
23162105 |
2013 |
Impaired cognition
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Polymorphism of the prion protein is associated with cognitive impairment in the elderly: the EVA study.
|
9748018 |
1998 |
Impaired cognition
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Effect of the angiotensin I-converting enzyme I/D polymorphism on cognitive decline. The EVA Study Group.
|
10794851 |
2000 |
Advanced breast cancer
|
0.020 |
Biomarker
|
disease |
BEFREE |
Correction 2: Everolimus (EVE) and exemestane (EXE) in patients with advanced breast cancer aged ≥ 65 years: new lessons for clinical practice from the EVA study.
|
30613355 |
2018 |
Advanced breast cancer
|
0.020 |
Biomarker
|
disease |
BEFREE |
Everolimus (EVE) and exemestane (EXE) in patients with advanced breast cancer aged ≥ 65 years: new lessons for clinical practice from the EVA study.
|
30159129 |
2018 |
Nonsyndromic Deafness
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
By screening a cohort of phenotype-matched subjects and a cohort of HI subjects in whom WES had been performed previously, we identified two additional families with biallelic truncating variants of MPZL2.
|
29961571 |
2018 |
Nonsyndromic Deafness
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Here, we report a loss-of-function variant (c.72delA) in MPZL2 in three unrelated multiplex families from Turkey and Iran with autosomal recessive nonsyndromic hearing loss.
|
29982980 |
2018 |
Alopecia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.
|
19054061 |
2009 |