Disease Directory

Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young is a type of Fanconi syndrome in which a mutation in the HNF4A gene is the un...

Information about the overview is currently limited for this condition.

Far eastern spotted fever is a rare disease. Detailed information about this condition is currently limited in medical literature.

Far-East scarlet-like fever is a severe inflammatory disease that occurs sporadically and in outbreaks in Russia and Japan. It is caused by an infecti...

Farber lipogranulomatosis is a rare disorder that affects the way sphingolipids, a type of fat, are processed in the body. People with this condition...

Feingold syndrome is a rare inherited malformation syndrome. It is also known as oculo-digito-esophageal-duodenal (ODED) syndrome among other names. T...

Feingold syndrome type 1 (FS1) is a rare inheritable condition that affects the development of multiple parts of the body. It is known for features su...

Feingold syndrome type 2 is a rare inherited condition that mainly affects the bones and can lead to mild intellectual disabilities. People with this...

Felty syndrome is a severe form of rheumatoid arthritis, often called 'super rheumatoid' disease. It is defined by a triad of features: rheumatoid art...

Fibulo-ulnar hypoplasia-renal anomalies syndrome is a rare condition that affects bone and kidney development. It is marked by abnormal development of...

Fiedler's myocarditis is a rare disease. Detailed information about this condition is currently limited in medical literature.

Filippi syndrome is a very rare condition that affects many parts of the body. It is known for a smaller head size (microcephaly) and differences in t...

Fine-Lubinsky syndrome is a rare condition that affects many parts of the body. It is characterized by several distinct features including delays in p...

Finnish type amyloidosis is a rare inherited condition also known by many other names, including MERETOJA syndrome and gelsolin amyloidosis. This cond...

Finnish upper limb-onset distal myopathy is a rare genetic condition that primarily affects the muscles of the hands and arms. It is characterized by...

Fischer-Zirnsak progeroid syndrome is a rare, not well-characterized condition. The name suggests that it may share features with other progeroid synd...

Flinders island spotted fever is a disease linked to the bacteria Rickettsia honei. It is transmitted to people through bites from cayenne ticks (Ambl...

Floating-Harbor syndrome is a genetic developmental disorder that affects growth and development. It is mainly characterized by distinctive facial fea...

Flynn-Aird syndrome is a neuroectodermal disorder that affects several systems in the body, including the nervous, skin, skeletal, and glandular syste...

Foix-Alajouanine syndrome is a rare condition that affects the spinal cord. Also called subacute ascending necrotising myelitis, it occurs when the ve...