Fabry disease is a progressive, multisystemic lysosomal storage disorder that primarily affects the blood vessels, heart, kidneys, skin, and nervous s...

Facial arteriovenous malformation is a vascular anomaly that affects the facial region and is characterized by abnormal direct communications between...

Facial cleft, also known as cleft face, craniofacial cleft, or prosoposchisis, is a congenital condition characterized by an opening or gap in the fac...

Facial dermoid cyst is a rare, benign skin growth that typically appears as a firm, nonpulsatile mass on the face. It is characterized by the presence...

Facial diplegia with paresthesias is a variant of Guillain-Barre syndrome that primarily affects the peripheral nerves controlling facial muscles. Ind...

Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome is an extremely rare condition that presents with distinctive facial features, re...

Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome is a developmental disorder primarily affectin...

Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome is an extremely rare condition marked by a combination of brain malformation...

Facial hemiatrophy, also known as progressive hemifacial atrophy or Romberg syndrome, is an acquired condition characterized by a slow, unilateral was...

Facial neuralgia is a neurological condition characterized by chronic or recurrent episodes of facial pain that primarily involve the nerves responsib...

Facial paresis, hereditary congenital, 3 is a condition present at birth that primarily affects facial movement and is associated with variable hearin...

Faciocardiorenal syndrome is a very rare condition that primarily affects multiple organ systems, including the brain, heart, and kidneys. It is chara...

Faciodigitogenital syndrome is a developmental disorder that affects facial features, limb structure, and genital development, often leading to a disp...

Facioscapulohumeral muscular dystrophy is an autosomal dominant disorder that mainly affects the muscles of the face, shoulder blade, and upper arms....