eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| laryngocele | ||||
| Disease ID | 1468 |
|---|---|
| Disease | laryngocele |
| Definition | Congenital anomalous dilitation of the laryngeal saccule that may extend internally into the airway or externally through the thyrohyoid membrane. |
| Synonym | congenital laryngocele congenital laryngocele (disorder) laryngoceles |
| Orphanet | |
| ICD10 | |
| UMLS | C0265761 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1468 |
|---|---|
| Disease | laryngocele |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:7) HP:0030731 | Carcinoma | 5 HP:0002860 | Squamous cell carcinoma | 2 HP:0012118 | Cancer of the larynx | 2 HP:0002664 | Neoplasia | 1 HP:0002781 | Upper airway obstruction | 1 HP:0011034 | Amyloid disease | 1 HP:0001609 | Hoarseness | 1 |
| Disease ID | 1468 |
|---|---|
| Disease | laryngocele |
| 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 | 1468 |
|---|---|
| Disease | laryngocele |
| Case | (Waiting for update.) |