ID

45019

Beskrivning

Principal Investigator: Jerry Kim, MD, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA MeSH: Malignant Hyperthermia https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000405 Malignant hyperthermia (MH) is a genetic disorder that causes a profound metabolic derangement following exposure to certain anesthetics. While approximately half of all cases are associated with ryanodine receptor-1 gene (RYR1) mutations, many cases have an unknown genetic cause. We sought to identify rare variants in novel MH candidate genes by sequencing the protein-coding regions of the genomes of individuals whose disease was either ruled in or out by the gold-standard diagnostic test. We also carefully selected individuals from well-characterized families to use gene-sharing information and maximize efficiency in the study design. Exome sequencing has helped identify the causes of over a dozen Mendelian disorders, has high power at low sample sizes, and is cost-efficient compared to whole-genome sequencing.

Länk

https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000405

Nyckelord

  1. 2022-07-13 2022-07-13 - Dr. Christian Niklas
  2. 2022-10-12 2022-10-12 - Adrian Schulz
Rättsinnehavare

Jerry Kim, MD, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA

Uppladdad den

13 juli 2022

DOI

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Licens

Creative Commons BY 4.0

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dbGaP phs000405 Next Generation Mendelian Genetics: Malignant Hyperthermia

Eligibility Criteria

Inclusion and exclusion criteria
Beskrivning

Inclusion and exclusion criteria

Inclusion Criteria:
Beskrivning

Inclusion Criteria

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
Positive IVCT biopsy
Beskrivning

Positive IVCT biopsy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1446409
UMLS CUI [1,3]
C0005558
UMLS CUI [1,4]
C1533691
UMLS CUI [1,5]
C0009917
UMLS CUI [1,6]
C0871511
Positive family history for MH
Beskrivning

Positive family history for MH

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0241889
UMLS CUI [1,3]
C0024591
Exclusion Criteria:
Beskrivning

Exclusion Criteria

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
Minor aged subject
Beskrivning

Minor aged subject

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0001779
Genetic variant in known causal gene
Beskrivning

Genetic variant in known causal gene

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0314603
UMLS CUI [1,3]
C0205419
UMLS CUI [1,4]
C0017337
UMLS CUI [1,5]
C0085978
Other familial muscle or metabolic disorders
Beskrivning

Other familial muscle or metabolic disorders

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0851352
UMLS CUI [1,3]
C0026845
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C0851352
UMLS CUI [2,3]
C0025517

Similar models

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion and exclusion criteria
Inclusion Criteria
Item
Inclusion Criteria:
boolean
C1512693 (UMLS CUI [1,1])
Positive IVCT biopsy
Item
Positive IVCT biopsy
boolean
C1512693 (UMLS CUI [1,1])
C1446409 (UMLS CUI [1,2])
C0005558 (UMLS CUI [1,3])
C1533691 (UMLS CUI [1,4])
C0009917 (UMLS CUI [1,5])
C0871511 (UMLS CUI [1,6])
Positive family history for MH
Item
Positive family history for MH
boolean
C1512693 (UMLS CUI [1,1])
C0241889 (UMLS CUI [1,2])
C0024591 (UMLS CUI [1,3])
Exclusion Criteria
Item
Exclusion Criteria:
boolean
C0680251 (UMLS CUI [1,1])
Minor aged subject
Item
Minor aged subject
boolean
C0680251 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
Genetic variant in known causal gene
Item
Genetic variant in known causal gene
boolean
C0680251 (UMLS CUI [1,1])
C0314603 (UMLS CUI [1,2])
C0205419 (UMLS CUI [1,3])
C0017337 (UMLS CUI [1,4])
C0085978 (UMLS CUI [1,5])
Other familial muscle or metabolic disorders
Item
Other familial muscle or metabolic disorders
boolean
C0680251 (UMLS CUI [1,1])
C0851352 (UMLS CUI [1,2])
C0026845 (UMLS CUI [1,3])
C0680251 (UMLS CUI [2,1])
C0851352 (UMLS CUI [2,2])
C0025517 (UMLS CUI [2,3])

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