ORPHA:101944
Rare pulmonary disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare pulmonary disease | |
| fr | Maladie pulmonaire rare | |
| de | Lungenkrankheit, seltene | |
| es | Enfermedad pulmonar rara | |
| it | Malattia polmonare rara | |
| nl | Zeldzame longziekte | |
| pt | Doença pulmonar, rara | |
| pl | Rzadkie choroby płuc | |
| cs | Vzácné plicní onemocnění | |
| uk | Рідкісне легеневе захворювання | |
| zh | 罕见肺部疾病 | |
| tr | Nadir akciğer hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15118 | E | validated | |
| UMLS | C5681796 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:97955Rare respiratory disease
rare respiratory diseases
Children (46):
- ORPHA:178320Acute lung injury
- ORPHA:1164Allergic bronchopulmonary aspergillosis
- ORPHA:60Alpha-1-antitrypsin deficiency
- ORPHA:99981Apnea of prematurity
- ORPHA:454836Avian influenza
- ORPHA:1303Bronchiolitis obliterans
- ORPHA:661Congenital central hypoventilation syndrome
- ORPHA:2140Congenital diaphragmatic hernia
- ORPHA:586Cystic fibrosis
- ORPHA:90060Diffuse alveolar hemorrhage
- ORPHA:171700Diffuse panbronchiolitis
- ORPHA:2903Familial spontaneous pneumothorax
- ORPHA:99803Haddad syndrome
- ORPHA:330012High altitude pulmonary edema
- ORPHA:60033Idiopathic bronchiectasis
- ORPHA:70590Infantile apnea
- ORPHA:182095Interstitial lung disease
- ORPHA:389Langerhans cell histiocytosis
- ORPHA:70588Meconium aspiration syndrome
- ORPHA:576074Middle East respiratory syndrome
- ORPHA:505248Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders
- ORPHA:685082Pediatric acute respiratory distress syndrome
- ORPHA:439881Plastic bronchitis
- ORPHA:449266Pleural empyema
- ORPHA:90066Pneumonia caused by Pseudomonas aeruginosa infection
- ORPHA:289390Primary Sjögren disease
- ORPHA:244Primary ciliary dyskinesia
- ORPHA:247522Primary ciliary dyskinesia-retinitis pigmentosa syndrome
- ORPHA:645814Primary pulmonary tuberculosis
- ORPHA:2038Pulmonary arteriovenous malformation
- ORPHA:217080Pulmonary fungal infections in patients deemed at risk
- ORPHA:60026Pulmonary nodular lymphoid hyperplasia
- ORPHA:411703Pulmonary non-tuberculous mycobacterial infection
- ORPHA:692812RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome
- ORPHA:293987Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome
- ORPHA:60032Recurrent respiratory papillomatosis
- ORPHA:425120STING-associated vasculopathy with onset in infancy
- ORPHA:140896Severe acute respiratory syndrome
- ORPHA:3167Siegler-Brewer-Carey syndrome
- ORPHA:36238Staphylococcal necrotizing pneumonia
- ORPHA:168593Sudden infant death-dysgenesis of the testes syndrome
- ORPHA:228426Syndromic multisystem autoimmune disease due to Itch deficiency
- ORPHA:90291Systemic sclerosis
- ORPHA:3348Tracheobronchopathia osteochondroplastica
- ORPHA:505395Ventilator-induced diaphragmatic dysfunction
- ORPHA:3471Young syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:2112OBSOLETE: Follicular hamartoma-alopecia-cystic fibrosis syndrome referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101944
- This record as JSON: /data/d/101944.json