Familial porphyria cutanea tarda

Autosomal dominant

Familial syringomyelia

Autosomal dominant, Autosomal recessive

Infancy, Neonatal

Feingold syndrome type 1

Autosomal dominant

Antenatal, Neonatal

Feingold syndrome type 2

Autosomal dominant

Antenatal, Neonatal

Fetal Gaucher disease

Autosomal recessive

Infancy, Neonatal

Fetal lung interstitial tumor

Infancy, Neonatal

Fibrohistiocytic inflammatory pseudotumor of the liver

Adult, Elderly

Fibromuscular dysplasia of the arteries of the extremities

Not applicable

Fibromuscular dysplasia of the cervical and intracranial arteries

Not applicable

Fibromuscular dysplasia of the coronary arteries

Not applicable

Fibromuscular dysplasia of the renal arteries

Not applicable

Fibromuscular dysplasia of the visceral arteries

Not applicable

Fibrotic hypersensitivity pneumonitis

Not applicable

Fish-eye disease

Autosomal recessive

Adolescent, Adult

Focal facial dermal dysplasia type I

Autosomal dominant

Antenatal, Neonatal

Focal facial dermal dysplasia type II

Autosomal dominant

Antenatal, Neonatal

Focal facial dermal dysplasia type III

Autosomal dominant, Autosomal recessive

Antenatal, Neonatal

Focal facial dermal dysplasia type IV

Autosomal recessive

Antenatal, Neonatal

Focal stiff limb syndrome

Not applicable

Adult

Foodborne botulism

All ages

Free sialic acid storage disease, infantile form

Autosomal recessive

Antenatal, Neonatal

Frontal encephalocele

Antenatal, Infancy, Neonatal

Furuncular myiasis due to Cordylobia anthropophaga

All ages

Furuncular myiasis due to Cordylobia rodhaini

All ages