Directory
Pyruvate carboxylase deficiency
Pyruvate carboxylase (PC) deficiency is a rare inherited disorder associated with a deficiency of the enzyme pyruvate carboxylase, which is...
Prekallikrein deficiency
Prekallikrein deficiency is a rare inherited disorder caused by a deficiency of prekallikrein, the precursor to...
Prolidase deficiency
Prolidase deficiency is a hereditary disorder caused by a deficiency of the enzyme prolidase, which is involved in metabolic processes...
Properdin deficiency
Properdin deficiency is a rare genetic disorder caused by a malfunction of the complement system - ...
Protein C deficiency
Protein C deficiency (PCD) is an inherited condition characterized by a significant decrease or absence of functional activity of protein...
Prothrombin deficiency
Prothrombin deficiency, or hypoprothrombemia, is a pathological condition characterized by an insufficient concentration of pro...
Pseudocholinesterase deficiency
Pseudocholinesterase deficiency is a genetic disorder associated with insufficient activity of the enzyme pseudocholinesterase...
Platelet storage pool deficiency
Platelet storage pool deficiency (PSD) is a condition characterized by a deficiency of platelets in the bone marrow and ...
Purine nucleoside phosphorylase deficiency
Purine nucleoside phosphorylase deficiency (PNP) is a rare but serious inherited disorder associated with metabolic...
Phosphoglycerate kinase deficiency
Phosphoglycerate kinase (PGK) deficiency is a rare inherited disorder characterized by a deficiency of the enzyme phosphoglycerate...
Phosphoglycerate mutase deficiency
Phosphoglycerate mutase deficiency (PGMD) is a rare, inherited metabolic disorder. It is a conditio...
Phosphomannoisomerase deficiency
Phosphomannoisomerase deficiency (PMI) is a rare inherited disorder caused by a deficiency in the enzyme responsible for catalyzing...
Pelvic floor dysfunction
Pelvic floor dysfunction is a complex condition associated with disruption of the anatomical and functional interaction of muscles, ligaments and ...
Coccygeal tract disease
A coccygeal cyst, or terminal cyst (pilonidal cyst), is an anomaly that occurs in the coccyx area, most often...
Peripheral arterial disease
Peripheral arterial disease (PAD) is a pathological condition characterized by atherosclerotic narrowing or...
Posterior urethral valves
Posterior urethral valves (PUVs) are abnormal anatomy of the posterior urethra characterized by the presence of valves or ...
Itchy Eustachian Tube
Itchy eustachian tube, also known as eustachitis, is an inflammatory condition of the eustachian tube, which connects the...
Pseudomonas Stutzeri infections
Pseudomonas stutzeri is a gram-negative bacterium belonging to the genus Pseudomonas that is widely distributed in the environm...
Red pityriasis versicolor
Pityriasis rubra pilaris, also known as trichophytosis rubra, is a dermatological disease caused by a fungus...
Pterygoid membrane of the conjunctiva and cornea
Pterygium is a degenerative change of the conjunctiva and cornea that appears as a triangular...
Palmoplantar keratoderma
Palmoplantar keratoderma (PPK) is a rare inherited disorder characterized by hyperkeratosis and thickening of the skin...
Pulmonary arteriovenous malformation (PAVM)
Pulmonary arteriovenous malformation (PAVM) is a congenital vascular disorder in which there is abnormal flow of blood...
Pulmonary arteriovenous fistula
Pulmonary arteriovenous fistula (PAVF) is a vascular anomaly characterized by confusion between arterial and venous...
Pulmonary veno-occlusive disease
Pulmonary veno-occlusive disease (PVOD) is a rare but serious disorder characterized by occlusion of the pulmonary veins, resulting in...
Pulmonary hypertension
Pulmonary hypertension (PH) is a pathological condition characterized by increased pressure in the pulmonary artery, which in...
Pulmonary sequestration
Pulmonary sequestration is a developmental abnormality of the lungs in which part of the lung tissue is functional but does not have normal...
Pulmonary alveolar proteinosis
Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by the accumulation of protein and lipids in the alveoli of the lungs, which causes...
Pulmonary supravalvular stenosis
Pulmonary supravalvular stenosis (PSVS) is a narrowing of the right ventricular outflow tract that interferes with the normal flow of blood...
Pulmonary nocardiosis
Pulmonary nocardiosis is an infectious disease caused by microorganisms of the genus Nocardia, which is characterized by the development of pulmonary...
Pol 3-associated leukodystrophy
Polymerase III (Pol 3)-associated leukodystrophy is a rare genetic disorder that affects the central...
