All terms in EFO
| Label | Id | Description |
|---|---|---|
| Psoas abscess | EFO_1001832 | [Abscess of the PSOAS MUSCLES resulting usually from disease of the lumbar vertebrae, with the pus descending into the muscle sheath. The infection is most commonly tuberculous or staphylococcal.] |
| pseudolymphoma | EFO_1001831 | [A neoplastic process that resembles a malignant lymphoma, but has a benign course.] |
| precursor T-cell lymphoblastic leukemia-lymphoma | EFO_1001830 | |
| Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 | MONDO_0020298 | |
| congenital pulmonary veins anomaly | MONDO_0020295 | [Aberrant drainage of one or more of the pulmonary veins which causes the return of oxygen-rich blood to the right atrium.] |
| respiratory aspiration | EFO_1001839 | [Inhaling liquid or solids, such as stomach contents, into the RESPIRATORY TRACT. When this causes severe lung damage, it is called ASPIRATION PNEUMONIA.] |
| renal nutcracker syndrome | EFO_1001838 | [Renal nutcracker syndrome (NCS) is a condition that occurs when the left renal vein (the vein that carries blood purified by the left kidney) becomes compressed between the aorta, abdominal and superior mesenteric artery. The signs and symptoms of the condition can vary from person to person. Some affected people may be asymptomatic while others develop severe and persistent symptoms. When present, features of NCS may include blood in the urine (hematuria), renovascular hypertension, varicose veins, orthostatic proteinuria, flank pain and/or abdominal pain. Some cases of mild NCS in children may be due to changes in body proportions associated with growth. Why NCS occurs or becomes symptomatic in adults is less clear. Treatment ranges from surveillance to surgical intervention and is based on the severity of symptoms and their expected reversibility when considering the affected person's age and stage of the syndrome., A rare, syndromic renal disease characterized by the entrapment of left renal vein (LRV) between the superior mesenteric artery (SMA) and the abdominal aorta, resulting in increased luminal pressure, renal hilar varices, hematuria and, at the microscopic level, rupture of thin-walled veins into the collecting system in renal fornices.] |
| rectocele | EFO_1001837 | [Herniation of the RECTUM into the VAGINA.] |
| pyogenic liver abscess | EFO_1001836 | [Single or multiple areas of PUS due to bacterial infection within the hepatic parenchyma. It can be caused by a variety of BACTERIA, local or disseminated from infections elsewhere such as in APPENDICITIS; CHOLECYSTITIS; PERITONITIS; and after LIVER TRANSPLANTATION.] |
| pyelocystitis | EFO_1001835 | [Inflammation of the KIDNEY PELVIS and the URINARY BLADDER.] |
| pyelitis | EFO_1001140 | [Inflammation of the renal pelvis., Inflammation of the KIDNEY PELVIS and KIDNEY CALICES where urine is collected before discharge, but does not involve the renal parenchyma (the NEPHRONS) where urine is processed.] |
| pulmonary aspergillosis | EFO_1001834 | [Infections of the respiratory tract with fungi of the genus ASPERGILLUS. Infections may result in allergic reaction (ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS), colonization in pulmonary cavities as fungus balls (MYCETOMA), or lead to invasion of the lung parenchyma (INVASIVE PULMONARY ASPERGILLOSIS)., A aspergillosis that involves the lung.] |
| Pubic Symphysis Diastasis | EFO_1001833 | [Separation of the PUBIC SYMPHYSIS. It is an uncommon complication of CHILDBIRTH causing postpartum PAIN, but it can also arise from other causes.] |
| obsolete_Carney triad | Orphanet_139411 | [Carney's triad is a rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas.] |
| obsolete_hereditary fructose intolerance | Orphanet_469 | |
| obsolete_non-acquired combined pituitary hormone deficiency | Orphanet_467 | |
| obsolete_fatal familial insomnia | Orphanet_466 | |
| obsolete_congenital plasminogen activator inhibitor type 1 deficiency | Orphanet_465 | |
| obsolete_incontinentia pigmenti | Orphanet_464 | |
| sinoatrial nodal reentry tachycardia | EFO_1001843 | [Abnormally rapid heartbeats caused by reentry circuit in or around the SINOATRIAL NODE. It is characterized by sudden onset and offset episodes of tachycardia with a HEART RATE of 100-150 beats per minute. The P wave is identical to the sinus P wave but with a longer PR interval.] |