Genetic Conditions - F

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Genetic Conditions…

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FA - Friedreich ataxia see Friedreich ataxia

Facial Injuries and Disorders

factor V Leiden thrombophilia

FALS see amyotrophic lateral sclerosis

Familial Acoustic Neuromas see neurofibromatosis 2

familial adenomatous polyposis

familial Alzheimer disease (FAD) see Alzheimer disease

familial amyotrophic lateral sclerosis see amyotrophic lateral sclerosis

familial dysautonomia

Familial Hemochromatosis see hemochromatosis

familial lipoprotein lipase deficiency

familial Mediterranean fever

Familial nonpolyposis colon cancer see hereditary nonpolyposis colorectal cancer

Familial PCT see porphyria cutanea tarda

familial pressure sensitive neuropathy see hereditary neuropathy with liability to pressure palsies

familial primary pulmonary hypertension (FPPH) see primary pulmonary hypertension

familial Turner syndrome see Noonan syndrome

Familial vascular leukoencephalopathy see CADASIL

FAP see familial adenomatous polyposis

FD see familial dysautonomia

Female Pseudo-Turner Syndrome see Noonan syndrome

Ferrochelatase deficiency see erythropoietic protoporphyria

ferroportin disease see hemochromatosis, type 4

Fever see familial Mediterranean fever

FGFR3-associated coronal synostosis see Muenke syndrome

fibrinoid degeneration of astrocytes see Alexander disease

Fibrocystic Disease of Pancreas see cystic fibrosis

Fibrofolliculomas with trichodiscomas and acrochordons see Birt-Hogg-Dubé syndrome

Fish malodor syndrome see trimethylaminuria

Fish odor syndrome see trimethylaminuria

FMF see familial Mediterranean fever

Folling Disease see phenylketonuria

fra(X) syndrome see fragile X syndrome

Fraccaro-Houston-Harris achondrogenesis see achondrogenesis, type 1B

fragile X syndrome

Fragilitas ossium see osteogenesis imperfecta

FRAXA Syndrome see fragile X syndrome

FRDA see Friedreich ataxia

Friedreich ataxia

FXS see fragile X syndrome