Directory
Pulmonary atresia with intact interventricular septum
Pulmonary artery atresia with intact interventricular septum (PAA with IVI) is a rare but serious congenital cardiovascular...
Plaque psoriasis
Plaque psoriasis is a chronic autoimmune condition characterized by excessive division of skin cells, resulting in the development of...
Painful swallowing
Painful swallowing, or odynophagia, is a symptom characterized by a feeling of pain or discomfort during the swallowing process....
Painful menstruation
Painful menstruation, or dysmenorrhea, is a condition characterized by severe pain that occurs in the pelvic area...
Pyle's disease
Pyle's disease, also known as stenosing ligamentitis or de Quervain's disease, is a progressive disorder characterized by...
Parkinson's disease
Parkinson's disease (PD) is a neurodegenerative disorder characterized by progressive loss of neurons in the substantia nigra, which...
Paget's disease of bone
Paget's disease of bone, also known as osteodystrophy or osteitis deformans, is a chronic skeletal disorder characterized by...
Paget's disease of the breast
Paget's disease of the breast (PDB) is a rare disorder characterized by erythema, eczema-like changes, and...
Peyronie's disease
Peyronie's disease, also known as fibroplasia of the corpus cavernosum, is a pathological condition characterized by the formation of...
Pelizaeus-Merzbacher disease
Pelizaeus-Merzbacher disease (PMD) is a rare inherited disorder that belongs to the group of myelinopathies. This disease is characterized by...
Pompe disease
Pompe disease (glycogen storage disease type II) is an inherited metabolic disorder caused by a deficiency of the enzyme acid glucose...
Variant Prinzmetal's angina
Variant Prinzmetal angina, also known as Prinzmetal's angina, is a syndrome characterized by episodic...
Parainfluenza virus type 3
Parainfluenza virus type 3 (HPIV-3) is a respiratory virus belonging to the Paramyxoviridae family. It is one of the ...
Funnel chest deformity
Pectus excavatum, or funnel chest deformity, is a developmental abnormality of the chest characterized by...
Inflammatory diseases of the pelvic organs
Pelvic inflammatory disease (PID) is a group of inflammatory conditions that affect the reproductive...
Congenital paramyotonia
Congenital paramyotonia is a rare hereditary disease characterized by a disorder of muscle function, which manifests itself in increased muscle...
Congenital pachyonychia
Pachyonychia congenita is a rare genetic disorder characterized by thickening and malformation of the nails, as well as hyperc...
Gangrenous pyoderma
Pyoderma gangrenosum (PG) is an inflammatory skin disease characterized by the appearance of painful ulcers that often quickly...
Parathyroid hyperplasia
Parathyroid hyperplasia is a pathological enlargement of the parathyroid tissues, which leads to excess...
Pediatric low-grade glioma (pLGG)
Childhood low-grade glioma (pLGG) is a group of brain tumors that typically occur in...
Childhood autoimmune neuropsychiatric disorders associated with streptococcal infections
Childhood autoimmune neuropsychiatric disorders associated with streptococcal infections are a group of diseases...
Childhood myocarditis
Childhood myocarditis is an inflammatory disease of the heart muscle (myocardium) that can occur at any age, but most often ...
PEPCK 1 deficiency
PEPCK (phosphoenolpyruvate carboxykinase) deficiency is a rare genetic disorder characterized by impaired energy metabolism...
Protein deficiency
Protein deficiency is a condition characterized by a level of protein intake that is insufficient to meet physical requirements.
Protein S deficiency
Protein S deficiency is a rare but potentially serious disorder associated with an increased risk of blood clots. Protein S is...
Growth hormone deficiency in children
Growth hormone deficiency (GHD) in children is a pathological condition characterized by insufficient synthesis of growth hormone (GH), produced by...
Peroxisomal acyl-CoA oxidase deficiency
Peroxisomal acyl-CoA oxidase deficiency (PAOD) is a rare inherited disorder characterized by impaired oxidative...
Pyridoxine deficiency
Pyridoxine deficiency, or vitamin B6, is a condition characterized by a lack of this vital nutrient in the body's...
Pyruvate dehydrogenase deficiency
Pyruvate dehydrogenase deficiency (EMDR) is a metabolic disorder caused by a deficiency of the enzyme pyruvate dehydrogenase, which...
Pyruvate decarboxylase deficiency
Pyruvate decarboxylase deficiency (PDC) is a rare metabolic disorder caused by a deficiency of the enzyme pyruvate...
