eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| bullous impetigo | ||||
| Disease ID | 1801 |
|---|---|
| Disease | bullous impetigo |
| Definition | Bullous Impetigo is a skin condition that characteristically occurs in the newborn, and is caused by a bacterial infection, presenting with bullae.[1]:256 - Wikipedia Reference: https://en.wikipedia.org/wiki/bullous impetigo |
| Synonym | bullous impetigo (disorder) bullous impetigo [ambiguous] impetigo bullosa impetigo bullosa (disorder) impetigo bullosa (disorder) [ambiguous] impetigo bullous impetigo contagiosa bullosa impetigo contagiosa of any site and any organism, bullous impetigo contagiosa, bullous impetigo, bullous |
| Orphanet | |
| ICD10 | |
| UMLS | C0021100 |
| SNOMED-CT | |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1801 |
|---|---|
| Disease | bullous impetigo |
| Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:8) HP:0010783 | Erythema HP:0100820 | Glomerulopathy HP:0005406 | Recurrent bacterial skin infections HP:0003095 | Septic arthritis HP:0100763 | Abnormality of the lymphatic system HP:0100806 | Sepsis HP:0008066 | Abnormal blistering of the skin HP:0200039 | Pustule |
| Text Mined Phenotype | (Waiting for update.) |
| Disease ID | 1801 |
|---|---|
| Disease | bullous impetigo |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:2) |
| Text Mined Symptom | (Waiting for update.) |
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:3) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0100763 | Abnormality of the lymphatic system | MP:0004502 | decreased incidence of tumors by chemical induction | lower than normal frequency of tumor incidence induced by one or more chemical carcinogens or mutagens |
| HP:0005406 | Recurrent bacterial skin infections | MP:0002412 | increased susceptibility to bacterial infection | greater likelihood that an organism will develop ill effects from a bacterial infection or from components of or toxins produced by bacteria |
| HP:0008066 | Abnormal blistering of the skin | MP:0009536 | abnormal interstitial cell of Cajal morphology | any structural anomaly in the type of cell found in the gastrointestinal tract and serving as a pacemaker that triggers gut contraction; ICCs mediate inputs from the enteric nervous system to smooth muscle cells and are thought to be the cells from which |
Mapped by homologous gene(Total Items:8) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0100763 | Abnormality of the lymphatic system | MP:0012431 | increased lymphoma incidence | greater than the expected number of neoplasms characterized by a proliferation of malignant lymphocytes in lymphoid tissue in a specific population in a given time period |
| HP:0100806 | Sepsis | MP:0011708 | decreased fibroblast cell migration | reduced frequency of or less rapid fibroblast cell migration that is accomplished by extension and retraction of a fibroblast pseudopodium |
| HP:0005406 | Recurrent bacterial skin infections | MP:0013799 | abnormal intestinal goblet cell physiology | any functional anomaly of the glandular simple columnar epithelial cell found in the mucosal lining of the small and large intestine, whose primary function is to secrete gel-forming mucins, the major components of mucus; intestinal goblet cells produce a |
| HP:0100820 | Glomerulopathy | MP:0014169 | decreased brown adipose tissue mass | decreased physical bulk or volume of brown adipose tissue |
| HP:0010783 | Erythema | MP:0013781 | abnormal mammary gland luminal epithelium morphology | any structural anomaly of the inner cell layer of the mammary epithelium bilayer that lines the luminal surface of mammary gland ducts and alveoli; luminal cells have only limited contact with the underlying basement membrane and surrounding connective ti |
| HP:0008066 | Abnormal blistering of the skin | MP:0020039 | increased bone ossification | increase in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance |
| HP:0003095 | Septic arthritis | MP:0010766 | abnormal NK cell physiology | any functional anomaly of a lymphocyte that can spontaneously kill a variety of target cells without prior antigenic activation via germline encoded activation receptors, and also regulate immune responses via cytokine release and direct contact with othe |
| HP:0200039 | Pustule | MP:0013745 | abnormal eyelid margin morphology | any structural anomaly of the confluence of the mucosal surface of the conjunctiva, the edge of the orbicularis, and the cutaneous epithelium |
| Disease ID | 1801 |
|---|---|
| Disease | bullous impetigo |
| Case | (Waiting for update.) |