형질
Honeycomb lung
Honeycombing represents destroyed and fibrotic lung tissue containing numerous cystic airspaces with thick fibrous walls, representing the late stage of various lung diseases, with complete loss of acinar architecture. The cysts range in size from a few millimeters to several centimeters in diameter, have variable wall thickness, and are lined by metaplastic bronchiolar epithelium. On chest radiographs, honeycombing appears as closely approximated ring shadows, typically 3-10 mm in diameter with walls 1-3 mm in thickness, that resemble a honeycomb; the finding implies end-stage lung disease. On CT scans, the appearance is of clustered cystic air spaces, typically of comparable diameters on the order of 3-10 mm but occasionally as large as 2.5 cm. Honeycombing is usually subpleural and is characterized by well-defined walls. It is a CT feature of established pulmonary fibrosis. Because honeycombing is often considered specific for pulmonary fibrosis and is an important criterion in the diagnosis of usual interstitial pneumonia, the term should be used with care, as it may directly impact patient care.
요약
- 다른 명칭
- Honeycomb cysts, Honeycombing
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이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/honeycomb-lung.json"
page <- fromJSON(url)
page$trait$name13 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.
- Familial Pulmonary FibrosisReads 5 of these genesPARNRTEL1SFTPA1SFTPA2TERTAbout this report →
- Dyskeratosis CongenitaReads 5 of these genesPARNRTEL1STN1TERCTERTAbout this report →
- Surfactant Metabolism DysfunctionReads 2 of these genesABCA3SFTPCAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
Show 9 more reports
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Epidermolysis BullosaReads 1 of these genesDSPAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesATP11AAbout this report →
- VitreoretinopathyReads 1 of these genesSTN1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSPAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesATP11AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesATP11AAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesDPP9About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesATP11AAbout this report →
연관 유전자 14개: Honeycomb lung
이 유전자들의 변화는 Honeycomb lung 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ABCA3ATP binding cassette subfamily A member 3 | 자주 (30–79%) | 질환 2개에서 나타남 |
| ATP11AATPase phospholipid transporting 11A | 자주 (30–79%) | 질환 1개에서 나타남 |
| DPP9dipeptidyl peptidase 9 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DSPdesmoplakin | 자주 (30–79%) | 질환 1개에서 나타남 |
| FAM13Afamily with sequence similarity 13 member A | 자주 (30–79%) | 질환 1개에서 나타남 |
| MUC5Bmucin 5B, oligomeric mucus/gel-forming | 자주 (30–79%) | 질환 1개에서 나타남 |
| PARNpoly(A)-specific ribonuclease | 자주 (30–79%) | 질환 2개에서 나타남 |
| RTEL1regulator of telomere elongation helicase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SFTPA1surfactant protein A1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SFTPA2surfactant protein A2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SFTPCsurfactant protein C | 자주 (30–79%) | 질환 1개에서 나타남 |
| STN1STN1 subunit of CST complex | 자주 (30–79%) | 질환 1개에서 나타남 |
| TERCtelomerase RNA component | 자주 (30–79%) | 질환 1개에서 나타남 |
| TERTtelomerase reverse transcriptase | 자주 (30–79%) | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
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