PedAM
Pediatric Disease Annotations & Medicines
| focal epithelial hyperplasia | ||||
| Disease ID | 1249 |
|---|---|
| Disease | focal epithelial hyperplasia |
| Definition | Hyperplasia of the mucous membrane of the lips, tongue, and less commonly, the buccal mucosa, floor of the mouth, and palate, presenting soft, painless, round to oval sessile papules about 1 to 4 mm in diameter. The condition usually occurs in children and young adults and has familial predilection, lasting for several months, sometimes years, before running its course. A viral etiology is suspected, the isolated organism being usually the human papillomavirus. (Jablonski, Illustrated Dictionary of Dentistry; Belshe, Textbook of Human Virology, 2d ed, p954) |
| Synonym | disease, heck disease, heck's epithelial hyperplasia, focal epithelial hyperplasias, focal feh, oral focal epithelial hyperplasia (morphologic abnormality) focal epithelial hyperplasia [disease/finding] focal epithelial hyperplasia of mouth focal epithelial hyperplasia of mouth (disorder) focal epithelial hyperplasia, oral focal epithelial hyperplasias heck dis heck disease heck's disease hecks dis hecks disease hyperplasia, focal epithelial hyperplasias, focal epithelial multifocal epithelial hyperplasia oral focal epithelial hyperplasia |
| OMIM | |
| DOID | |
| UMLS | C0206067 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:4) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:17) 1917 | EEF1A2 | DISEASES 123263 | MTFMT | DISEASES 8797 | TNFRSF10A | DISEASES 2735 | GLI1 | DISEASES 10343 | PKDREJ | DISEASES 2247 | FGF2 | DISEASES 7157 | TP53 | DISEASES 3549 | IHH | DISEASES 6469 | SHH | DISEASES 51206 | GP6 | DISEASES 2814 | GP5 | DISEASES 2253 | FGF8 | DISEASES 9218 | VAPA | DISEASES 2736 | GLI2 | DISEASES 3456 | IFNB1 | DISEASES 2737 | GLI3 | DISEASES 4700 | NDUFA6 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1249 |
|---|---|
| Disease | focal epithelial hyperplasia |
| Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:1) HP:0000153 | Abnormal mouth |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) HP:0002721 | Immunodeficiency | 1 HP:0012740 | Papilloma | 1 HP:0005550 | Chronic lymphatic leukemia | 1 |
| Disease ID | 1249 |
|---|---|
| Disease | focal epithelial hyperplasia |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |