A–Z DIRECTORY
Conditions beginning with F
- Fabry diseaseX-linked
- Facioscapulohumeral muscular dystrophyAutosomal dominant
- Factor V deficiencyAutosomal recessive
- Factor V Leiden thrombophiliaPattern unknown
- Factor VII deficiencyAutosomal recessive · Not inherited
- Factor X deficiencyNot inherited · Autosomal recessive
- Factor XI deficiencyAutosomal dominant · Autosomal recessive
- Factor XIII deficiencyAutosomal recessive
- Familial acute myeloid leukemia with mutated CEBPAAutosomal dominant
- Familial adenomatous polyposisAutosomal dominant, inherited from one affected parent
- Familial atrial fibrillationAutosomal dominant
- Familial candidiasisAutosomal dominant · Autosomal recessive
- Familial cold autoinflammatory syndrome type 2
- Familial dysautonomiaAutosomal recessive
- Familial encephalopathy with neuroserpin inclusion bodiesAutosomal dominant, inherited or a new variant
- Familial erythrocytosisAutosomal recessive · Autosomal dominant
- Familial exudative vitreoretinopathyAutosomal recessive · X-linked recessive · Autosomal dominant
- Familial focal epilepsy with variable fociAutosomal dominant
- Familial glucocorticoid deficiencyAutosomal recessive
- Familial HDL deficiencyAutosomal dominant
- Familial hemiplegic migraineAutosomal dominant
- Familial hemophagocytic lymphohistiocytosisAutosomal recessive
- Familial hyperaldosteronismAutosomal dominant
- Familial hypercholesterolemiaAutosomal recessive · Autosomal dominant
- Familial hypobetalipoproteinemiaAutosomal codominant
- Familial isolated hyperparathyroidismAutosomal dominant
- Familial isolated pituitary adenomaAutosomal dominant
- Familial lipoprotein lipase deficiencyAutosomal recessive
- Familial male-limited precocious pubertyAutosomal dominant
- Familial Mediterranean feverAutosomal dominant · Autosomal recessive
- Familial osteochondritis dissecansAutosomal dominant
- Familial paroxysmal kinesigenic dyskinesiaAutosomal dominant
- Familial paroxysmal nonkinesigenic dyskinesiaAutosomal dominant
- Familial partial lipodystrophyAutosomal dominant · Autosomal recessive
- Familial pityriasis rubra pilarisAutosomal dominant
- Familial porencephalyAutosomal dominant
- Familial restrictive cardiomyopathyAutosomal dominant
- Familial thoracic aortic aneurysm and dissectionAutosomal dominant
- Fanconi anemiaAutosomal recessive · X-linked · X-linked recessive · Autosomal dominant
- Farber lipogranulomatosisAutosomal recessive
- FarsightednessPattern unknown
- Fatty acid hydroxylase-associated neurodegenerationAutosomal recessive
- FBXL4-related encephalomyopathic mitochondrial DNA depletion syndromeAutosomal recessive
- Feingold syndromeAutosomal dominant
- FG syndromeX-linked recessive
- FibrochondrogenesisAutosomal recessive · Autosomal dominant
- Fibrodysplasia ossificans progressivaAutosomal dominant
- FibromyalgiaPattern unknown
- Fibronectin glomerulopathyAutosomal dominant
- Fish-eye diseaseAutosomal recessive
- Floating-Harbor syndromeAutosomal dominant
- Focal dermal hypoplasiaX-linked dominant
- FOXG1 syndromeAutosomal dominant
- FOXP2-related speech and language disorderAutosomal dominant, inherited or a new variant · Autosomal dominant
- Fragile X syndromeX-linked dominant
- Fragile X-associated primary ovarian insufficiencyX-linked dominant
- Fragile X-associated tremor/ataxia syndromeX-linked dominant
- Fragile XE syndromeX-linked
- Fraser syndromeAutosomal recessive
- Frasier syndromeAutosomal dominant
- Free sialic acid storage disorderAutosomal recessive
- Freeman-Sheldon syndromeAutosomal dominant · Autosomal recessive
- Friedreich ataxiaAutosomal recessive
- Frontometaphyseal dysplasiaX-linked dominant
- Frontonasal dysplasiaAutosomal dominant · Autosomal recessive
- Frontotemporal dementia with parkinsonism-17Autosomal dominant
- Fryns syndromeAutosomal recessive
- Fuchs endothelial dystrophyPattern unknown · Autosomal dominant
- FucosidosisAutosomal recessive
- Fukuyama congenital muscular dystrophyAutosomal recessive
- Fumarase deficiencyAutosomal recessive
- Fundus albipunctatusAutosomal recessive
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