Disease Directory

Fontaine farriaux blanckaert syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Fontaine progeroid syndrome is a rare premature aging syndrome that affects multiple organ systems, most the skin and craniofacial structures. It is c...

Fowler syndrome is a very rare condition with limited detailed information available. It is known by several names, including encephaloclastic prolife...

Franceschini Vardeu Guala syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Frank-Ter Haar syndrome is a very rare inherited condition that affects several body systems, especially the eyes, skeleton, heart, and facial develop...

Fraser syndrome is a rare condition that mainly presents with cryptophthalmos, where the skin covers the eyes, and syndactyly, which is the fusion of...

Fraser syndrome 1 is a rare condition that is also known by several other names such as cryptophthalmos with Other malformations and cryptophthalmos-s...

Fraser syndrome 2, also known as FRASRS2, is a rare genetic condition. Information about the overall definition of this condition is currently limited...

Fraser syndrome 3, also known as FRASRS3, is a rare condition that is recorded in genetic databases (OMIM:617667). Limited information is available ab...

Frasier syndrome is a rare condition characterized by the combination of male pseudohermaphrodism and glomerular nephropathy. This means that people w...

Freeman-Sheldon syndrome is a very rare condition that affects many parts of the body. It is known for multiple congenital contractures, which means t...

Freiberg disease is a rare condition that affects the long bones in the foot, most often the second or third metatarsal. It is most commonly seen duri...

Frey syndrome is an autonomic disorder that mostly affects the face and upper chest area. It is characterized by excessive sweating and sometimes faci...

Frias syndrome is a rare condition that results from a partial deletion on the long arm of chromosome 14. This genetic change can affect the developme...

Fried's tooth and nail syndrome, also known as ECTD8, ectodermal dysplasia 8, or the hair/tooth/nail type, is a rare genetic condition. Detailed infor...

Friedreich ataxia is an inherited neurological condition that primarily affects movement coordination and heart function. It is associated with pathog...

Friedreich ataxia 1 is a hereditary neurodegenerative condition that primarily affects the nervous system and coordination. It is caused by mutations...

Friedreich ataxia 2 is a subtype of Friedreich ataxia that has been linked to the region on chromosome 9p23-p11. The precise genetic basis is still un...

Friedreich ataxia with retained reflexes is a rare disease. Detailed information about this condition is currently limited in medical literature.

Information about overview is currently limited for this condition.