Total 15 clinical symptoms reported for Primary familial polycythemia due to EPO receptor mutation
| Abnormal hemoglobin |
Anomaly in the level or the function of hemoglobin, the oxygen-carrying protein of erythrocytes.
Synonyms:Abnormal Hb |
Very frequent |
| Dyspnea |
Difficult or labored breathing. Dyspnea is a subjective feeling only the patient can rate, e.g., on a Borg scale.
Synonyms:Abnormal breathing; Breathing difficulty; Difficult to breathe; Difficulty breathing; Shortness of breath; Trouble breathing |
Very frequent |
| Epistaxis |
Epistaxis, or nosebleed, refers to a hemorrhage localized in the nose.
Synonyms:Bloody nose; Frequent nosebleeds; Nasal hemorrhage; Nose bleed; Nose bleeding; Nosebleed |
Very frequent |
| Fatigue |
A subjective feeling of tiredness characterized by a lack of energy and motivation.
Synonyms:Fatigue; Tired; Tiredness |
Very frequent |
| Headache |
Cephalgia, or pain sensed in various parts of the head, not confined to the area of distribution of any nerve.
Synonyms:Headache; Headaches |
Very frequent |
| Polycythemia |
Polycythemia is diagnosed if the red blood cell count, the hemoglobin level, and the red blood cell volume all exceed the upper limits of normal.
Synonyms:Abnormally shaped erythrocytes; Erythrocytosis; Increased red blood cells; Polyglobulia |
Very frequent |
| Venous thrombosis |
Formation of a blood clot (thrombus) inside a vein, causing the obstruction of blood flow.
Synonyms:Blood clot in vein |
Very frequent |
| Vertigo |
An abnormal sensation of spinning while the body is actually stationary.
Synonyms:Dizzy spell |
Very frequent |