PedAM
Pediatric Disease Annotations & Medicines
| wandering spleen | ||||
| Disease ID | 1384 |
|---|---|
| Disease | wandering spleen |
| Definition | A condition characterized by an abnormal spleen position due to loss, weakness, or malformation of one or more of the ligaments that hold the spleen in its normal position in the left upper abdomen. It may present as a birth defect or follow injuries or pregnancy. Signs and symptoms include abdominal discomfort and splenomegaly. |
| Synonym | displaced spleen displaced spleens drifting spleen drifting spleens floating spleen floating spleens lien migrans lien migrans (disorder) lien mobilis ptoses, splenic ptosis, splenic spleen, displaced spleen, drifting spleen, floating spleen, wandering spleens, displaced spleens, drifting spleens, floating spleens, wandering splenic ptoses splenic ptosis splenoptoses splenoptosis wandering spleen (disorder) wandering spleen [disease/finding] wandering spleens |
| UMLS | C0272414 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:7) C0042961 | volvulus | 7 C0001173 | gastric outlet obstruction | 2 C0019284 | diaphragmatic hernia | 1 C0024796 | marfan syndrome | 1 C0037998 | splenic infarction | 1 C0018916 | haemangioma | 1 C0018824 | valvular heart disease | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1384 |
|---|---|
| Disease | wandering spleen |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:9) HP:0002580 | Volvulus | 7 HP:0002027 | Abdominal pain | 3 HP:0011458 | Abdominal symptom | 1 HP:0000085 | Horseshoe kidney | 1 HP:0001744 | Splenomegaly | 1 HP:0012531 | Pain | 1 HP:0001748 | Polysplenia | 1 HP:0000776 | Diaphragmatic hernia | 1 HP:0100790 | Hernia | 1 |
| Disease ID | 1384 |
|---|---|
| Disease | wandering spleen |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:3) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:2) |
Manually Genotype(Total Text Mining 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.) |
Chemical(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |