Fetal parvovirus syndrome is a condition that affects the developing fetus when a pregnant woman contracts parvovirus B19, an infection commonly assoc...

Fetal phenothiazine syndrome is a condition that has been identified in clinical settings, although detailed information remains limited. The availabl...

Fetal trimethadione syndrome is a drug-related embryofetopathy that occurs when a fetus is exposed to trimethadione during pregnancy. This condition i...

Fetal valproate syndrome is an anticonvulsant drug-related embryofetopathy that occurs when a fetus is exposed to valproic acid during pregnancy. The...

FGFR1-related Pfeiffer syndrome is a type of Pfeiffer syndrome that is caused by a mutation in the FGFR1 gene. This condition falls under the umbrella...

FGFR2-related Pfeiffer syndrome is a rare condition that is defined by a mutation in the FGFR2 gene. This gene plays an important role in bone develop...

FGFR3-related chondrodysplasia is a rare condition that is identified by its association with the FGFR3 terminology. Information about the features, d...

FG syndrome 1 is a rare genetic condition that is caused by a mutation in the MED12 gene. It is one member of the FG syndrome spectrum of disorders. M...

FHL1-related myopathy is a group of muscle disorders that includes conditions such as Emery-Dreifuss muscular dystrophy (EDMD), reducing body myopathy...

Fibrillary astrocytoma is the most frequent histological variant of diffuse astrocytoma, a type of brain tumor that arises from astrocytes. It is char...

Fibroblastic liposarcoma is a type of soft tissue cancer characterized by a fibroblastic component within the tumor. It falls under the category of li...

Fibrochondrogenesis is a severe skeletal dysplasia and chondrodysplasia that affects newborns, with a striking presentation at birth. It is linked to...

Fibrochondrogenesis 1 is a severe genetic disorder affecting skeletal development, caused by mutations in the COL11A1 gene. It involves abnormal forma...

Fibrochondrogenesis 2 is a skeletal disorder characterized by a range of distinctive bone and cartilage abnormalities. It is caused by pathogenic vari...

Fibrodysplasia ossificans progressiva (FOP) is a severe heritable disorder of connective tissue that primarily affects the skeletal and muscular syste...

Fibrolamellar hepatocellular carcinoma is a distinctive form of liver cancer that arises in non-cirrhotic livers, predominantly affecting younger pati...