FOXG1 disorder is a neurodevelopmental condition that primarily affects brain growth and function, leading to significant cognitive and motor challeng...

Fragile X-associated tremor/ataxia syndrome is a neurodegenerative condition primarily affecting the central nervous system, with a characteristic adu...

Fragile X syndrome is a neurodevelopmental condition primarily affecting the nervous and skeletal systems, characterized by intellectual and behaviora...

Currently, there are no identified genes associated with fragile X syndrome type 1, and the inheritance pattern remains unestablished. This lack of de...

Fragile X syndrome type 2 is a condition that appears to affect neurodevelopment and may impact learning and behavior. Although detailed definitions a...

Fragile X syndrome type 3 is a condition that affects neurodevelopment, although detailed information about its clinical presentation remains limited....

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...

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

FRAXE intellectual disability is a form of nonsyndromic X-linked intellectual disability (NS-XLMR) that is characterized by a mild intellectual defici...

FRAXF syndrome is a rare condition that was first identified in a family where several members had developmental delay. The initial report noted an ex...

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...

Free sialic acid storage disease is a lysosomal storage disorder that encompasses a spectrum of neurological and developmental challenges. It is assoc...

Free sialic acid storage disease, infantile form is a metabolic condition that predominantly presents in infancy. It is associated with pathogenic var...

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...