AtlasTrait
Progressive pulmonary function impairment
Summary
- Body system
- Abnormality of the respiratory system
AtlasThis page as data
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library(jsonlite)
url <- "https://dantelabs.com/traits/progressive-pulmonary-function-impairment.json"
page <- fromJSON(url)
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Get my Genome Test18 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.
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 2 of these genesSMARCB1SMARCE1About this report →
- NeurofibromatosisReads 2 of these genesNF2SMARCB1About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
Show 14 more reports
- Pulmonary Alveolar MicrolithiasisReads 1 of these genesSLC34A2About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesSUFUAbout this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFBAbout this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Kidney CancerReads 1 of these genesBAP1About this report →
- Urinary and Renal System TumourReads 1 of these genesBAP1About this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesSMPD1About this report →
- Intellectual DisabilityReads 1 of these genesSMARCB1About this report →
Read the genes linked to Progressive pulmonary function impairment, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Progressive pulmonary function impairment
Changes in these genes cause rare conditions in which Progressive pulmonary function impairment 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 |
|---|---|---|
| SMPD1sphingomyelin phosphodiesterase 1 | Often (30–79%) | In 1 condition |
| AKT1AKT serine/threonine kinase 1 | Rarely (1–4%) | In 1 condition |
| BAP1BRCA1 associated deubiquitinase 1 | Rarely (1–4%) | In 1 condition |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Rarely (1–4%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Rarely (1–4%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Rarely (1–4%) | In 1 condition |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Rarely (1–4%) | In 1 condition |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Rarely (1–4%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Rarely (1–4%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Rarely (1–4%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Rarely (1–4%) | In 1 condition |
| TRAF7TNF receptor associated factor 7 | Rarely (1–4%) | In 1 condition |
| SLC34A2solute carrier family 34 member 2 | Not recorded | In 1 condition |
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.
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 2026.10.17-8666dff2.
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