Changes in corneal membranes

H7_CORNEALMEMBRANE

corneal disease: A non-neoplastic or neoplastic disorder that affects the cornea. Representative examples include keratitis, bullous keratopathy, and squamous cell carcinoma.

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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 H18.3
  • Cause of death: ICD-10 H18.3

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

89

4. Check minimum number of events

None

89

5. Include endpoints

None

89

6. Filter based on genotype QC (FinnGen only)

89

Control definitions (FinnGen only)

Control exclude
H7_SCLERACORNEA

Extra metadata

Level in the ICD hierarchy
4
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
H18
Name in latin
Abnormitates membranarum cornealium

Case counts by codes

FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

-FinRegistry-

Key figures

All Female Male
Number of individuals
Whole population 414 262 151
Only index persons 402 255 147
Unadjusted period prevalence (%)
Whole population 0.01 0.01 0.00
Only index persons 0.01 0.01 0.01
Median age at first event (years)
Whole population 61.95 63.82 58.75
Only index persons 61.37 62.88 58.75

-FinnGen-

Key figures

All Female Male
Number of individuals 89 62 27
Unadjusted period prevalence (%) 0.02 0.02 0.01
Median age at first event (years) 63.62 63.48 63.94

-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

No data

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.

Matched cohort

Matched cases
72
Matched controls
721
Code
Vocabulary
Description
Odds Ratio
-log10(p)
N matched cases
N matched controls
H18.3
ICD-10 Finland
Changes in corneal membranes
+∞
103.4
72
*
H18.5
ICD-10 Finland
Hereditary corneal dystrophies
253.0
19.5
19
*
CG2T4
NOMESCO Finland
Topography assessment of cornea
+∞
17.4
16
*
S01XA20
ATC
artificial tears and other indifferent preparations; ophthalmic
8.8
15.3
57
217
CG2X4
NOMESCO Finland
Optical coherence tomography (OCT) of cornea
+∞
12.9
12
*
H16.0
ICD-10 Finland
Corneal ulcer
63.8
9.9
11
*
XCW99
NOMESCO Finland
Other investigative procedure of eye
8.1
9.8
23
39
CG2S4
NOMESCO Finland
Photography of cornea
+∞
9.6
9
*
Z96.1
ICD-10 Finland
Presence of intraocular lens
6.8
8.7
23
46
CK2X4
NOMESCO Finland
Optical coherence tomography (OCT) of ocular fundus
8.5
8.2
18
27
H16.9
ICD-10 Finland
Keratitis, unspecified
+∞
6.3
6
*
H18.4
ICD-10 Finland
Corneal degeneration
+∞
6.3
6
*
H20.0
ICD-10 Finland
Acute and subacute iridocyclitis
+∞
6.3
6
*
ZXA10
NOMESCO Finland
Bilateral
4.3
6.1
24
74

Mortality – FinRegistry

Association

Association between endpoint H7_CORNEALMEMBRANE and mortality.

Females

No data

Males

No data

Mortality risk

Mortality risk for people of age

years, who have H7_CORNEALMEMBRANE.

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

Index endpoint: H7_CORNEALMEMBRANE – Changes in corneal membranes

GWS hits: -

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