Fazio Londe syndrome
Fazio-Londe syndrome: A rare inherited motor neuron disease characterized by progressive muscle weakness which ultimately leads to premature death.
Diseases
Fealty syndrome
A rare complication of long-term rheumatoid arthritis which involves an enlarged spleen and blood abnormalities.
Febrile Ulceronecrotic Mucha-Habermann disease
A very rare skin disease characterized by bleeding skin ulcers and fever. There is no obvious cause of the condition. The skin ulcers spread and can cover most of the body.
Fechtner syndrome
A rare condition characterized by the presence of large blood platelets, kidney inflammation, deafness and abnormal leukocytes.
Feigenbaum Bergeron Richardson syndrome
A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries.
Feigenbaum Bergeron syndrome
Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Feigenbaum bergeron syndrome as a "rare disease".
Feingold Trainer syndrome
A very rare syndrome characterized mainly by short stature, mental retardation, cleft palate and facial anomalies.
Felty’s Syndrome
Felty's syndrome is a complication of long-standing rheumatoid arthritis. Felty's syndrome is defined by the presence of three conditions: rheumatoid arthritis, an enlarged spleen (splenomegaly), and an abnormally low white blood count. Felty's syndrome is uncommon. It affects less than 1% of patients with rheumatoid arthritis.
Female pseudohermaphrodism
A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
Female pseudohermaphrodism Genuardi type
Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Female pseudohermaphrodism genuardi type as a "rare disease".
Femoral facial syndrome
A rare genetic disorder characterized by underdeveloped femur, short nose and cleft palate.
Femur bifid with monodactylous ectrodactyly
A rare condition characterized by a thigh bone split into two and missing fingers resulting in a lobster-claw shaped hand (ectrodactyly).
Femur fibula ulna syndrome
A very rare syndrome characterized mainly by abnormalities of the thigh, forearm and calf bone. The degree of abnormality and number of limbs involved is variable. The upper limbs are affected more than the lower limbs and the right side is affected more than the left side.
Fenton Wilkinson Toselano syndrome
A rare syndrome characterized mainly by ataxia, light sensitivity and short stature.
Ferlini Ragno Calzolari syndrome
Fernhoff Blackston Oakley syndrome
A very rare syndrome characterized mainly by retarded fetal growth and jaw anomaly as well as various other abnormalities.
Fertile eunuch syndrome
Fetal acitretin syndrome
Fetal exposure to Acitretin (Soriatane, NeoTigason) can result in malformations. Acitretin is a retoind drug often used to treat psoriasis .
Fetal akinesia syndrome X-linked
A rare syndrome where the fetus is unable to move or has reduced mobility due to brain defects.
Fetal akinesia syndrome- X-linked
A rare syndrome where the fetus is unable to move or has reduced mobility due to brain defects.
Fetal alcohol syndrome
Fetal alcohol syndrome is growth, mental, and physical problems that may occur in a baby when a mother drinks alcohol during pregnancy.A pattern of mental and physical birth defects caused by excessive alcohol use during pregnancy. The range and severity of the symptoms may vary greatly.
Fetal aminopterin syndrome
A rare disorder which produces multiple abnormalities and results from a failed abortion attempt using the drugs aminopterin and methotrexate.
Fetal and neonatal alloimmune thrombocytopenia
Neonatal Alloimmune Thrombocytopenia (NAIT) is a blood-related disease that affects expectant mothers and their babies.
Most people are familiar with the red blood cells that make up the majority of the blood in our bodies, but may not be aware of a second type of cell in our blood stream called platelets. These small cells are responsible for stopping bleeding in the human body.
Neonatal Alloimmune Thrombocytopenia is a disease that develops when platelets in the pregnant mother and her baby become incompatible and cannot exist together.
Fetal anticonvulsant syndrome
Maternal use of anticonvulsants may increase the risk of the fetus developing birth defects. There is insufficient evidence to definitely conclude that maternal use of anticonvulsants is harmful to the fetus.
Fetal antihypertensive drugs syndrome
Fetal brain disruption sequence
A very rare syndrome characterized by skull and brain abnormalities.
Fetal cytomegalovirus syndrome
A rare condition where a fetus becomes infected with the cytomegalovirus through the mother.
Fetal diethylstilbestrol syndrome
Fetal diethylstilbestrol syndrome (medical condition): A very rare syndrome characterized mainly caused by exposure to diethylstilbestrol (used to prevent complications during pregnancy such as miscarriage and prematurity) during pregnancy.