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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/emphysema.json"
page <- fromJSON(url)
page$trait$nameEmphysemaHP:0002097
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Get my Genome Test38 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Cutis LaxaReads 9 of these genesEFEMP2FBLN5LTBP4LTBP1ELNALDH18A1About this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Alpha-1 Antitrypsin DeficiencyReads 1 of these genesSERPINA1About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
Show 34 more reports
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 3 of these genesSCNN1ASCNN1BSCNN1GAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesEVCEVC2About this report →
- Marfan Like SyndromesReads 2 of these genesFBN1TGFB2About this report →
- Aortic AneurysmReads 2 of these genesFBN1TGFB2About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Systemic Lupus ErythematosusReads 1 of these genesDNASE1L3About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Familial Pulmonary FibrosisReads 1 of these genesNAF1About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesFBLN5LMNAAbout this report →
- Autoimmune DiseaseReads 1 of these genesDNASE1L3About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL3A1About this report →
- Dyskeratosis CongenitaReads 1 of these genesNAF1About this report →
- Other Inborn Errors of ImmunityReads 3 of these genesSPINK5FOXN1TAP1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesFBLN5LMNANDUFAF6About this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesFOXN1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesATP6V0A2About this report →
- Male InfertilityReads 1 of these genesCFTRAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGLAAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesALDH18A1About this report →
- Leigh SyndromeReads 1 of these genesNDUFAF6About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesATP6V0A2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFAF6About this report →
- Epilepsy (Full Panel)Reads 1 of these genesATP6V1AAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesALDH18A1About this report →
Read the genes linked to Emphysema, and the rest of your genome, with one test.
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Get my Genome Test43 genes linked to Emphysema
Changes in these genes cause rare conditions in which Emphysema is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Always | In 2 conditions |
| FBLN5fibulin 5 | Always | In 3 conditions |
| FBN1fibrillin 1 | Always | In 2 conditions |
| LTBP4latent transforming growth factor beta binding protein 4 | Always | In 1 condition |
| COL3A1collagen type III alpha 1 chain | Very often (80–99%) | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| LTBP1latent transforming growth factor beta binding protein 1 | Very often (80–99%) | In 1 condition |
| SERPINA1serpin family A member 1 | Very often (80–99%) | In 1 condition |
| CDT1chromatin licensing and DNA replication factor 1 | Often (30–79%) | In 1 condition |
| ELNelastin | Often (30–79%) | In 2 conditions |
| GLAgalactosidase alpha | Often (30–79%) | In 1 condition |
| GMNNgeminin DNA replication inhibitor | Often (30–79%) | In 1 condition |
| NAF1nuclear assembly factor 1 ribonucleoprotein | Often (30–79%) | In 1 condition |
| ORC1origin recognition complex subunit 1 | Often (30–79%) | In 1 condition |
| RHOHras homolog family member H | Often (30–79%) | In 1 condition |
| TSC1TSC complex subunit 1 | Often (30–79%) | In 1 condition |
| TSC2TSC complex subunit 2 | Often (30–79%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sometimes (5–29%) | In 1 condition |
| BTNL2butyrophilin like 2 | Sometimes (5–29%) | In 2 conditions |
| CFTRCF transmembrane conductance regulator | Sometimes (5–29%) | In 1 condition |
| DNASE1L3deoxyribonuclease 1L3 | Sometimes (5–29%) | In 1 condition |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Sometimes (5–29%) | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Sometimes (5–29%) | In 1 condition |
| GLI1GLI family zinc finger 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 2 conditions |
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sometimes (5–29%) | In 1 condition |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Sometimes (5–29%) | In 1 condition |
| SCNN1Asodium channel epithelial 1 subunit alpha | Sometimes (5–29%) | In 1 condition |
| SCNN1Bsodium channel epithelial 1 subunit beta | Sometimes (5–29%) | In 1 condition |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Sometimes (5–29%) | In 1 condition |
| SONSON DNA and RNA binding protein | Sometimes (5–29%) | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Sometimes (5–29%) | In 1 condition |
| TGFB2transforming growth factor beta 2 | Sometimes (5–29%) | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Not recorded | In 2 conditions |
| ATP6V1AATPase H+ transporting V1 subunit A | Not recorded | In 1 condition |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Not recorded | In 1 condition |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Not recorded | In 1 condition |
Show 3 more genes
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.18-8b139e39.
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