Directory
Satoyoshi syndrome
Satoyoshi syndrome (Satoyoshi symptom) is a rare disorder characterized by a combination of clinical manifestations, including n...
Swyer syndrome
Swyer syndrome (or monochromosomal syndrome) is a rare genetic disorder caused by a disorder in the formation of...
Swyer-James syndrome
Swyer-James syndrome (also known as pulmonary hypoplasia or isolated pulmonary hypoplasia syndrome) is a rare...
Sezary syndrome
Sezary syndrome (Sezary-Hopkins syndrome) is a rare and aggressive disease belonging to the group of lymphomas, which manifests itself in...
Seckel syndrome
Seckel syndrome (Seckel malaria) is a rare genetic disorder characterized by specific developmental and functional disorders of the...
Sengers syndrome
Sengers syndrome is a rare genetic disorder that belongs to a group of disorders that involve abnormalities in the structure and function of the...
Senior-Loken syndrome
Senior-Loken syndrome is a rare genetic disorder characterized by a combination of two main pathologies: retino...
Simpson-Golabi-Bemel syndrome
Simpson-Golabi-Bemel syndrome (GBS) is a rare inherited disorder that belongs to a group of developmental defects associated with...
Singleton-Merten syndrome
Singleton-Merten syndrome (SMS) is a rare genetic disorder characterized by multiple systemic abnormalities...
Scott's syndrome
Scott syndrome (or Kostolanyi syndrome) is a rare genetic disorder characterized by developmental abnormalities,...
Smith-Kingsmore syndrome
Smith-Kingsmore syndrome is a rare genetic disorder characterized by multiple congenital...
Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome (SLO) is a rare inherited metabolic disorder characterized by impaired synthesis of ...
Smith-Magenis syndrome
Smith-Magenis syndrome (SMS) is a rare genetic disorder caused by a deletion or mutation in the RAI1 gene. The diseas...
Snyder-Robinson syndrome
Snyder-Robinson syndrome (SRS) is a rare genetic disorder that involves abnormal muscle...
Sotos syndrome
Sotos syndrome is a rare genetic disorder that belongs to a group of syndromes associated with premature aging. The diseas...
Sturge-Weber syndrome
Sturge-Weber syndrome (SWS) is a rare congenital disorder characterized by a combination of vascular anomalies, n...
Stevens-Johnson syndrome
Stevens-Johnson syndrome (SJS) is a rare but serious disorder that involves a severe hypersensitivity reaction to...
Stickler syndrome
Stickler syndrome is a genetic disorder characterized by abnormalities in connective tissue resulting from mutations in...
Stormorken Syndrome
Stormorken syndrome is a rare genetic disorder characterized by multiple clinical manifestations...
Stuve-Wiedemann syndrome
Stuve-Wiedemann syndrome is a rare genetic disorder that belongs to a group of disorders involving...
Susak's syndrome
Susac syndrome is a rare autoimmune disease characterized by a combination of neurological, ophthalmological and neuropsychiatric...
Saethre-Chotzen syndrome
Saethre-Chotzen syndrome (SCS) is a rare genetic disorder characterized by a combination of neurological and cardiac...
Shapiro syndrome
Shapiro syndrome is a rare hereditary disease characterized by the manifestation of various endocrine and neurological disorders...
Schwartz-Jampel syndrome
Schwartz-Jampel syndrome (SDS) is a rare genetic disorder characterized by abnormalities associated with various...
Shwachman-Diamond syndrome
Shwachman-Diamond syndrome (SDS) is a rare inherited disorder characterized by impaired hematopoiesis and function...
Sjogren's syndrome
Sjogren's syndrome is a chronic systemic autoimmune disease characterized by preferential involvement of the exocrine...
Sjögren-Larsson syndrome
Sjogren-Larsson syndrome (SLS) is a hereditary disorder characterized by a combinatorial defect of the sebaceous glands, p...
Schinzel-Giedion syndrome
Schinzel-Gideon syndrome (Syndrome of Shinzawa-Gideon) is a rare genetic disorder characterized by the presence of multiple congenital...
Sheehan's syndrome
Sheehan's syndrome (or postpartum hypopituitarism) is a rare but serious complication that occurs due to massive ...
Schnitzler syndrome
Schnitzler syndrome (Schinzel-Giedion syndrome) is a rare genetic disorder that affects multiple body systems...
