eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| tracheobronchomalacia | ||||
| Disease ID | 1600 |
|---|---|
| Disease | tracheobronchomalacia |
| Definition | A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the TRACHEA and the BRONCHI. This results in a floppy non-rigid airway making patency difficult to maintain. |
| Synonym | chondromalacia of trachea and bronchi syndrome, williams-campbell tracheobronchomalacia (disorder) tracheobronchomalacia [disease/finding] tracheobronchomalacias williams campbell syndrome williams-campbell syndrome |
| Orphanet | |
| OMIM | |
| UMLS | C0340231 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C0024115 | lung disease | 2 C0006267 | bronchiectasis | 1 C0018799 | heart disease | 1 C0152021 | congenital heart disease | 1 C0014850 | esophageal atresia | 1 C0002726 | amyloidosis | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1600 |
|---|---|
| Disease | tracheobronchomalacia |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:9) HP:0002955 | Granulomatosis | 1 HP:0011034 | Amyloid disease | 1 HP:0002097 | Pulmonary emphysema | 1 HP:0002575 | Tracheoesophageal fistula | 1 HP:0012735 | Coughing | 1 HP:0030828 | Wheezing | 1 HP:0002032 | Esophageal atresia | 1 HP:0002110 | Bronchiectasis | 1 HP:0006528 | Chronic lung disease | 1 |
| Disease ID | 1600 |
|---|---|
| Disease | tracheobronchomalacia |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:3) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
All Snps(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
|---|
| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
|---|
| (Waiting for update.) |
| Disease ID | 1600 |
|---|---|
| Disease | tracheobronchomalacia |
| Case | (Waiting for update.) |