Senile cataract

disease
On this page

Summary

Senile cataract (MONDO:0004847) is a disease with 30 GWAS associations across 13 studies and 10 clinical trials. A subtype of cataract — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 30
  • Clinical trials: 10

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namesenile cataract
Mondo IDMONDO:0004847
DOIDDOID:9669
ICD-10-CMH25
NCITC35012
SNOMED CT39450006
UMLSC0036646
MedGen11372
Is cancer (heuristic)no

Data availability: 30 GWAS associations (13 studies).

Disease family

This is a subtype of cataract. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › disorder of orbital regioneye disorderlens disordercataractsenile cataract

Related subtypes (28): immature cataract, diabetic cataract, mature cataract, tetanic cataract, myotonic cataract, diabetes mellitus type 2 associated cataract, cataract 4 multiple types, cataract 29, cataract 1 multiple types, early-onset non-syndromic cataract, cataract 3 multiple types, cataract 9 multiple types, cataract 28, cataract 18, cataract 12 multiple types, cataract 34 multiple types, cataract 36, bhaskar jagannathan syndrome, autosomal dominant cataract, craniostenosis cataract, Kozlowski Rafinski Klicharska syndrome, cataract 49, cataract 48, hypermature cataract, nuclear cataract, cortical cataract, cataract 2, multiple types, cataract 50 with or without glaucoma

Subtypes (2): cortical senile cataract, nuclear senile cataract

Genetics & variants

GWAS landscape

30 GWAS associations across 13 studies. Top hits map to 2 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
chr20:194961212e-26A0.12
chr7:461746552e-20G0.08
chr11:1873821e-19T0.11
chr11:691763953e-19C0.12
chr4:1739840491e-16T0.83
chr9:222069881e-15T0.07
rs348724712e-15TCF7L2T0.04
chr15:282884193e-15C0.08
chr3:1816502402e-14GT0.06
chr17:816192017e-13T0.06
chr7:1273750292e-12A0.19
chr1:2270141703e-11G0.05
chr16:74106984e-11G0.06
chr17:1371984e-10C0.12
chr20:106690377e-10AAAT0.06
chr11:658505671e-09A1.85
chr17:831077113e-09T0.05
chr10:1224541646e-09A0.06
chr8:94571131e-08C0.84
chr2:2175317371e-08G0.05
chr1:1690719332e-08C0.05
chr17:638761182e-08C0.89
chr7:1257930193e-08C0.53
chrX:670869463e-08A2.23
chr6:1634314934e-08C0.05
chr14:438148834e-08A0.23
chr17:139993864e-08G2.29
chr16:866751355e-08A0.05
chrX:651025615e-08A1.86
rs562164352e-07SDK2?

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90477674Verma A2024197,600206,486Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90477673Verma A202453,12953,452Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480071Verma A202453,12953,452Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90473410UK Biobank Whole-Genome Sequencing Consortium202534,058424,382Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667821UK Biobank Whole-Genome Sequencing Consortium202534,058424,382Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90477671Verma A202420,66033,135Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90435987Zhou W20188,369388,609Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
GCST90651926Liu TY20255,960223,893Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population.
GCST90477672Verma A20242,1974,058Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90726851Kim HI20261,25242,774Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic30

MAF distribution

BucketVariants
common (>=0.05)2
low_freq (0.01-0.05)0
rare (<0.01)0
unknown28

Functional consequences

ConsequenceCount
unknown28
intron_variant2

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
chr20:194961212e-26Tier 4: intronic/intergenic
chr7:461746552e-20Tier 4: intronic/intergenic
chr11:1873821e-19Tier 4: intronic/intergenic
chr11:691763953e-19Tier 4: intronic/intergenic
chr4:1739840491e-16Tier 4: intronic/intergenic
chr9:222069881e-15Tier 4: intronic/intergenic
rs3487247110112994312T>C0.296intron_variantTCF7L22e-15Tier 4: intronic/intergenic
chr15:282884193e-15Tier 4: intronic/intergenic
chr3:1816502402e-14Tier 4: intronic/intergenic
chr17:816192017e-13Tier 4: intronic/intergenic
chr7:1273750292e-12Tier 4: intronic/intergenic
chr1:2270141703e-11Tier 4: intronic/intergenic
chr16:74106984e-11Tier 4: intronic/intergenic
chr17:1371984e-10Tier 4: intronic/intergenic
chr20:106690377e-10Tier 4: intronic/intergenic
chr11:658505671e-09Tier 4: intronic/intergenic
chr17:831077113e-09Tier 4: intronic/intergenic
chr10:1224541646e-09Tier 4: intronic/intergenic
chr8:94571131e-08Tier 4: intronic/intergenic
chr2:2175317371e-08Tier 4: intronic/intergenic
chr1:1690719332e-08Tier 4: intronic/intergenic
chr17:638761182e-08Tier 4: intronic/intergenic
chr7:1257930193e-08Tier 4: intronic/intergenic
chrX:670869463e-08Tier 4: intronic/intergenic
chr6:1634314934e-08Tier 4: intronic/intergenic
chr14:438148834e-08Tier 4: intronic/intergenic
chr17:139993864e-08Tier 4: intronic/intergenic
chr16:866751355e-08Tier 4: intronic/intergenic
chrX:651025615e-08Tier 4: intronic/intergenic
rs562164351773457507C>A,G,T0.05intron_variantSDK22e-07Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 10.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified10

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02966496Not specifiedUNKNOWNSafety and Efficacy of Implantation of Two Multifocal Intraocular Lenses in the Treatment of Senile Cataract
NCT03050008Not specifiedCOMPLETEDEfficacy of FLACS USFREE Compared to Traditional Surgery Using Ultrasound.
NCT03262285Not specifiedCOMPLETEDCorneal Endothelial Cell Loss After Phacoemulsification Compared With Extracapsular Cataract Extraction
NCT03766230Not specifiedUNKNOWNClinical Study on Second-eye Pain in Cataract Surgery
NCT04468308Not specifiedUNKNOWNVRQOL in Cataract Patients During the COVID-19 Pandemic
NCT04972435Not specifiedCOMPLETEDEffect of Multifocal Intraocular Lens on Contrast Sensitivity in Primary Angle-Closure Patients
NCT05014269Not specifiedCOMPLETEDPhacoemulsification in Patients With Corneal Opacities
NCT05646004Not specifiedCOMPLETED621 Real World Study
NCT06192901Not specifiedCOMPLETEDSafety and Performance of Hydrophobic and Hydrophilic Intraocular Lenses After Bilateral Cataract Surgery
NCT06383754Not specifiedCOMPLETEDClareon Intraocular Lens Stability in Vitrectomy Patients: CLOVE Study

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.