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...

Friedreich ataxia is an inherited condition that primarily affects the nervous system, musculature, and skeletal system, leading to progressive proble...

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.

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...

Frontal convexity meningioma is a type of meningioma that primarily affects the frontal sulcus region of the brain. Although specific age of onset and...

Frontal lobe ependymal tumor is a brain neoplasm arising from ependymal cells, the specialized cells that line the ventricles, and it specifically aff...

Frontal sinus cancer is a malignant tumor that originates in the frontal sinus, one of the paranasal sinuses near the forehead. As a type of head and...

Frontal sinus neoplasm refers to a tumor arising in the frontal sinus and can be either benign or malignant. The condition encompasses a range of tumo...

Frontal sinus squamous cell carcinoma is a malignant tumor arising from the mucosal surface of the frontal sinus. It affects the epithelial lining of...

Frontofacionasal dysplasia is a congenital condition affecting the craniofacial region, characterized by a spectrum of anomalies such as brachycephaly...

Frontometaphyseal dysplasia (FMD) is a condition within the otopalatodigital syndrome spectrum, primarily affecting skeletal development and facial st...

Frontometaphyseal dysplasia 1 is a rare skeletal dysplasia that primarily affects the skeletal system while also involving the ear and nervous system....