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This is a non-core endpoint: only basic statistics are computed.

See these related core endpoints for full statistics:

Disorders of sulfur-bearing amino-acid metabolism

Endpoint Browser

E4_SULFURMET

Endpoint definition

↥

Endpoint definition steps

FinnGen

Phenotype data

520210

1. Apply sex-specific rule

None

520210

2. Check conditions

None

520210

3. Check pre-conditions, main-only, mode, registry filters

Registry filters:

  • Hospital discharge: ICD-10 — E72.1
  • Hospital discharge: ICD-9 — 2704
  • Hospital discharge: ICD-8 — 7082
  • Cause of death: ICD-10 — E72.1
  • Cause of death: ICD-9 — 2704
  • Cause of death: ICD-8 — 7082

2 out of 7 registries used, show all original rules.

12

4. Check minimum number of events

None

12

5. Include endpoints

None

12

6. Filter based on genotype QC (FinnGen only)

12

Control definitions (FinnGen only)

Control exclude
E4_METABOLIA

Extra metadata

Level in the ICD hierarchy
4
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
E72
Name in latin
Perturbationes metabolismi acidorum aminoicorum sulfuratorum

Case counts by codes

↥

FinnGen case counts by registry codes:

Not enough data for upset plot.

Full data table

Summary Statistics

↥

-FinRegistry-

Key figures

All Female Male
Number of individuals
Whole population 151 75 75
Only index persons 104 52 52
Unadjusted period prevalence (%)
Whole population 0.00 0.00 0.00
Only index persons 0.00 0.00 0.00
Median age at first event (years)
Whole population 51.19 48.55 53.31
Only index persons 42.24 39.59 44.89

-FinnGen-

Key figures

All Female Male
Number of individuals 12 8 -
Unadjusted period prevalence (%) 0.00 0.00 -
Median age at first event (years) 45.97 43.41 -

-FinRegistry-

Age distribution of first events

-FinnGen-

Age distribution of first events

-FinRegistry-

Year distribution of first events

-FinnGen-

Year distribution of first events

-FinRegistry-

Cumulative Incidence Function

No data

-FinnGen-

Cumulative Incidence Function

Not a core endpoint, no data to show.

CodeWAS (R11)

↥

CodeWAS is a tool for exploring the associations between an endpoint and all of the medical codes and drug codes.

This is a new tool, please reach out using the contact form for feedback and improvement ideas.

First, a cohort is built by matching controls to the endpoint cases using year of birth and sex. Then, a Fisher test is done for all the medical codes and drug codes between the cases and controls of this cohort. Codes are reported in the table below if they have −log10(p-value) ≥ 6.

No data available

LabWAS

↥
OMOP Concept
People with measurements
Mean N measurements
Mean measured value
(ID) Name
N Cases
N Controls
OR
-log10(p)
cases
controls
cases
controls
unit
-log10(p)
N cases
N controls
5
7
11.10
2.84
2.8
1.4
4.6
12.3
mmol/l
—
5
7
5
7
11.10
2.84
1.8
1.3
11.6
12.0
g/l
—
5
7
5
7
11.10
2.84
2.0
1.4
—
—
—
0
0
5
10
7.64
2.32
2.6
1.5
—
—
—
0
0
7
27
4.75
1.90
12.7
5.7
—
—
—
0
0
6
22
4.39
1.70
5.7
1.8
—
—
—
0
0
5
18
3.99
1.45
1.6
1.5
—
—
—
0
0
5
20
3.53
1.30
5.4
2.6
—
—
—
0
0
5
21
3.33
1.23
6.6
3.4
92.2
93.7
%
—
5
21
5
24
2.83
0.87
1.8
2.8
—
—
—
0
0
6
39
2.06
0.47
3.3
2.1
—
—
—
0
0
5
35
1.73
0.29
7.6
5.2
—
1.2
—
0
9
0
10
0.00
0.22
0.0
3.2
—
—
—
0
0
0
10
0.00
0.22
0.0
1.7
—
—
—
0
0
7
63
1.26
0.11
4.3
3.2
—
—
—
0
0
0
5
0.00
0.00
0.0
1.0
—
—
—
0
0
0
5
0.00
0.00
0.0
1.8
—
—
—
0
0
0
5
0.00
0.00
0.0
1.8
—
—
—
0
0
0
7
0.00
0.00
0.0
1.1
—
1.2
—
0
7
0
5
0.00
0.00
0.0
1.6
—
—
—
0
0
0
6
0.00
0.00
0.0
1.8
—
—
—
0
0
0
6
0.00
0.00
0.0
2.0
—
—
—
0
0
0
5
0.00
0.00
0.0
1.0
—
—
—
0
0
0
6
0.00
0.00
0.0
1.2
—
0.3
—
0
6

Mortality – FinRegistry

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Association

Association between endpoint E4_SULFURMET and mortality.

Females

No data

Males

No data

Mortality risk

Mortality risk for people of age

years, who have E4_SULFURMET.

N-year risk Females Males
1 No data No data
5 No data No data
10 No data No data
15 No data No data
20 No data No data

Relationships between endpoints

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Index endpoint: E4_SULFURMET – Disorders of sulfur-bearing amino-acid metabolism

GWS hits: -

Endpoint
Case Overlap
Survival Analysis
Genetic Correlations
Genetic Signals
N (Jaccard index)
HR [CI]
rg [CI]
Hits
Coloc Hits
FinRegistry
FinnGen
FinRegistry
FinnGen
FinnGen
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