Disease Index
9,486 diseasesprimary plasmacytoma of the bone
human disease
primary polyarteritis nodosa
human disease
primary progressive aphasia
progressive language and speech disorder
MeSH: D018888
primary progressive apraxia of speech
human disease
primary progressive freezing gait
human disease
primary pulmonary hypertension
chronic pulmonary heart disease characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, among others, has symptoms shortness of breath, dizziness, fainting, leg swelling
MeSH: D065627
primary pulmonary lymphoma
primary qualitative or quantitative defects of alpha-dystroglycan
human disease
primary renal tubular acidosis
human disease
Primary Sclerosing Cholangitis
Primary sclerosing cholangitis is a chronic cholestatic liver disease characterized by inflammation and fibrosis of intrahepatic and extrahepatic bile ducts, leading to biliary cirrhosis. Approximately 60-80% of patients have concurrent inflammatory bowel disease, particularly ulcerative colitis. The condition carries increased risk for cholangiocarcinoma (10-15% lifetime risk). Prevalence is estimated at 6-16 per 100,000 in Northern European populations.
ICD: K83.01MeSH: D015209
primary short bowel syndrome
human disease
primary syringomyelia
human disease
Primary systemic amyloidosis
disease caused by the accumulation of abnormal proteins
Primary tumors of the heart
Any of the forms of heart neoplasm that have a rare incidence
primary unilateral adrenal hyperplasia
primitive neuroectodermal tumor of the cervix uteri
human disease
primitive neuroectodermal tumor of the corpus uteri
primitive neuroectodermal tumor that involves the body of uterus
Primrose syndrome
medical condition
MeSH: C536420
PRKAR1B-related neurodegenerative dementia with intermediate filaments
human disease
proboscis
facial anomaly
progenism
malocclusion in which the mandible is anterior to the maxilla as reflected by the first relationship of the first permanent molar (mesioclusion)
MeSH: D008313
progeria
genetic disorder that causes early aging
MeSH: D011371
progeria-associated arthropathy
human disease
progeria-short stature-pigmented nevi syndrome
Progeria-short stature-pigmented nevi is a progeroid disorder characterised by low birthweight, short stature, multiple pigmented nevi and lack of facial subcutaneous fat
MeSH: C536422
progeroid features-hepatocellular carcinoma predisposition syndrome
human disease
progeroid syndrome
range of genetic disorders which cause a person to appear to grow older faster
MeSH: D019588
progeroid syndrome, Petty type
human disease
progressive bifocal chorioretinal atrophy
Progressive bifocal chorioretinal atrophy (PBCRA) is an early-onset chorioretinal dystrophy characterized by large atrophic macular and nasal retinal lesions, nystagmus, myopia, poor vision, and slow disease progression
MeSH: C535356
progressive cavitating leukoencephalopathy
progressive cerebello-cerebral atrophy
human disease