Disease Directory

Polymerase proofreading-related adenomatous polyposis, also known as PPAP, is a rare condition identified in specialized medical databases such as Orp...

Pontiac fever is a mild form of legionellosis that shows flu-like symptoms. People with this condition may experience nausea, muscle aches, fever, cou...

Potocki-Lupski syndrome, also known as 17p11.2 Duplication syndrome or 17p11.2 microduplication syndrome, is a rare genetic condition. It occurs becau...

Potocki-Shaffer syndrome is a rare genetic condition that has been reported in 23 individuals from 14 families. People with this syndrome often show f...

Powassan encephalitis is a rare disease caused by infection with the Powassan virus. This condition affects the brain, resulting in inflammation and p...

PrP systemic amyloidosis is an extremely rare genetic disorder that was previously known as chronic diarrhea with hereditary sensory and autonomic neu...

Prader-Willi syndrome is a complex neurodevelopmental condition that alters the function of multiple body systems, particularly the brain’s hypothalam...

Information about overview is currently limited for this condition. Prader-Willi syndrome due to imprinting mutation is recognized in established rare...

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 is a rare form of a genetic disorder known as Prader-Willi syndrome. In this...

Prader-Willi syndrome due to paternal 15q11q13 deletion is a complex neurodevelopmental condition that affects multiple organ systems, including the e...

Information about overview is currently limited for this condition.

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 is a complex condition that primarily affects neurodevelopment, endocrine function,...

Prader-Willi syndrome due to translocation is a complex neurodevelopmental disorder that results from abnormal genomic imprinting and disrupted parent...

Prader-Willi-like syndrome is an uncommon genetic condition that affects multiple body systems and mimics many features of classical Prader-Willi synd...

Prata-Liberal-Goncalves syndrome, also known as acrodysplasia scoliosis or brachydactyly-scoliosis-carpal fusion syndrome, is a very rare genetic cond...

Preaxial polydactyly of toes, also known by names such as bifid great toes and bifid hallux, is a rare congenital condition affecting the structure of...

Preaxial polydactyly of toes, bilateral is a rare condition affecting the structure of the toes. In this condition, people may have a splitting or dup...

Preaxial polydactyly of toes, unilateral is a rare congenital condition. This condition involves an abnormality in the development of the great toe on...

Preeyasombat-Varavithya syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Prieto syndrome is a rare genetic condition that is characterized by an intellectual deficit along with unique facial features. People with this condi...