Directory
Familial multiple lipomatosis
Familial multiple lipomatosis is a genetic disorder characterized by the formation of multiple lipomas - good...
Familial multiple nevus of Flammei
Familial multiple nevus Flammei (from the Latin "flamma" - "flame") is a rare genetic disease that manifests itself in...
Familial neurocardiogenic syncope
Familial neurocardiogenic syncope is a syndrome characterized by transient loss of consciousness caused by dysfunction of the autonomic nervous system.
Familial otosclerosis
Familial otosclerosis is a hereditary disease characterized by abnormal growth of bone tissue in the area of...
Familial periodic paralysis
Familial periodic paralysis (FPP) is an inherited disorder characterized by episodes of paralysis that occur in...
Familial progressive cardiac conduction defect
Familial progressive cardiac conduction defect (FPCCD) is an inherited disorder characterized by a...
Familial pancreatic cancer
Familial pancreatic cancer is a relatively rare but serious disease that is associated with a high incidence of ...
Familial prostate cancer
Familial prostate cancer is a malignant neoplasm that develops in the tissues of the prostate gland. This pathology is most common in ...
Familial atypical multiple melanoma syndrome
Familial atypical multiple melanoma syndrome (FAMMM syndrome) is an inherited disorder characterized by a pre...
Familial transthyretin amyloidosis
Familial transthyretin amyloidosis (familial ATTR amyloidosis) is an inherited disorder characterized by delayed...
Familial cold autoinflammatory syndrome
Familial cold autoinflammatory syndrome (FCAS) is an inherited autoimmune disorder characterized by epi...
Familial chronic mucocutaneous candidiasis
Familial chronic mucocutaneous candidiasis (FCMC) is a rare, inherited disease caused by genetic factors in children...
FOXG1 syndrome
FOXG1 syndrome is a rare inherited disorder caused by mutations in the FOXG1 gene, located on chromosome 1...
FG syndrome
FH syndrome (phenylhydrazine type) is a rare genetic disorder that is associated with a disorder of amino acid metabolism...
Feingold syndrome
Feingold syndrome (or Feingold-Mendel syndrome, depending on the author's preference) is a rare genetic diseas...
Fanconi syndrome
Fanconi syndrome is a rare inherited disorder characterized by abnormal function of the renal proximal tubules.
Fanconi-Bickel syndrome
Fanconi-Bickel syndrome (FBS) is a rare inherited disorder characterized by impaired ability of the kidneys to regenerate blood.
Felty's syndrome
Felty syndrome is a relatively rare but serious autoimmune disease that presents with a complex of clinical manifestations...
Philippi syndrome
Philippi syndrome is a rare inherited disorder that involves changes in glucose metabolism and can lead to...
Fitz-Hugh-Curtis syndrome
Fitz-Hugh-Curtis syndrome, also known as "liver fever" phenomenon, is a rare inflammatory disorder characterized by...
Fontan syndrome
Fontan syndrome is a rare inherited disorder characterized by a combination of various abnormalities, including but not limited to...
Frank Ter Haar syndrome
Frank ter Haar syndrome, also known as Chromosome 6 syndrome, is a rare genetic disorder characterized by multiple...
Fraser syndrome
Fraser Syndrome is a rare genetic disorder characterized by multiple abnormalities in the ...
Frey's syndrome
Frey syndrome, also known as choreic blindness or oral hyperhidrosis syndrome, is a rare neurogenic disorder that occurs in...
Freeman Sheldon syndrome
Freeman-Sheldon syndrome (FSS) is a rare genetic disorder characterized by abnormalities in the development of the facial and con...
Freeman-Sheldon syndrome
Freeman-Sheldon syndrome is a rare genetic disorder characterized by abnormalities in the development of the facial structures...
Fryns syndrome
Fryns syndrome, also known as incomplete boyish Edwards syndrome, is a rare genetic disorder that...
Femur-Fibula-Ulna Syndrome
Femur-fibula-ulna syndrome (FFULS) is a rare structural disorder characterized by...
Fragile X syndrome
Fragile X syndrome (FXS) is an inherited disorder associated with a syndrome caused by a mutation in the FMR1 gene, localized in the...
Fetal parvovirus syndrome
Fetal parvovirus syndrome (FPS) is a congenital disorder resulting from fetal infection with parvovirus B1...
