Conditions Search
Conditions starting from Fa to Fe
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'Fa to Fe' returned 175 records
- Fabry Disease
- FACES Syndrome
- Facial Ectodermal Dysplasia
- Faciocardiorenal Syndrome
- Faciodigitogential syndrome
- Faciogential dysplasia
- Faciomandibular Myoclonus, Nocturnal
- Facioscapulohumeral muscular dystrophy
- Factor H deficiency
- Factor I Deficiency
- Factor II
- Factor II Deficiency
- Factor v and factor viii, combined deficiency of, 1
- Factor v and factor viii, combined deficiency of, 2
- Factor V Deficiency
- Factor V Leiden (FVL)
- Factor V Leiden thrombophilia
- Factor VII Deficiency
- Factor VIII deficiency
- Factor X Deficiency
- Factor X Deficiency, Congenital
- Factor XI Deficiency
- Factor XI Deficiency, Congenital
- Factor XII Deficiency
- Factor XIII deficiency
- Factor xiii, a subunit, deficiency of
- Factor xiii, b subunit, deficiency of
- Failure of tooth eruption, primary
- Fairbank Disease
- Fallopian Tube Cancer
- Fallot Complex with Severe Mental and Growth Retardation
- Familial adenomatous polyposis
- Familial Amyloid Polyneuropathy
- Familial amyloidosis, Finnish type
- Familial Aortic Dissection
- Familial aplasia of the vermis
- Familial atrial myxoma
- Familial Atypical Multiple Mole Melanoma Syndrome
- Familial avascular necrosis of the femoral head
- Familial benign hypercalcemia
- Familial benign pemphigus
- Familial bilateral striatal necrosis
- Familial cancer of breast
- Familial Cold Autoinflammatory Syndrome
- Familial Cold Autoinflammatory Syndrome (FCAS)
- Familial cold autoinflammatory syndrome 2
- Familial cold autoinflammatory syndrome 3
- Familial cold urticaria
- Familial Cold Urticaria Syndrome
- Familial Colorectal Cancer
- Familial Congenital Fourth Cranial Nerve Palsy
- Familial Cylindromatosis
- Familial Deafness
- Familial Dermographism
- Familial Dilated Cardiomyopathy
- Familial Dysautonomia
- Familial Ectopia Lentis
- Familial ectopic ossification
- Familial emphysema
- Familial Encephalopathy with Neuroserpin Inclusion Bodies
- Familial Eosinophilia
- Familial Erythrocytosis, 1
- Familial expansile osteolysis
- Familial exudative vitreoretinopathy
- Familial febrile seizures 8
- Familial gynecomastia, due to increased aromatase activity
- Familial Hemiplegic Migraine
- Familial hemiplegic migraine type 3
- Familial Hypercholesterolemia
- Familial hyperinsulinism
- Familial Hypersecretion of Adrenal Androgens
- Familial Hypersensitivity Pneumonitis
- Familial hypertriglyceridemia
- Familial Hypertrophic Cardiomyopathy
- Familial hypoalphalipoproteinemia
- Familial Hypobetalipoproteinemia (FHBL)
- Familial hypocalciuric hypercalcemia
- Familial hypokalemia-hypomagnesemia
- Familial Hypophosphatemic Rickets
- Familial Hypopituitarism
- Familial idiopathic basal ganglia calcification
- Familial infantile myasthenia
- Familial interstitial pulmonary fibrosis
- Familial isolated hyperparathyroidism
- Familial joint laxity
- Familial juvenile gout
- Familial juvenile hyperuricaemic nephropathy
- Familial Mediterranean fever
- Familial mediterranean fever, autosomal dominant
- Familial melanoma
- Familial multiple lipomatosis
- Familial Multiple Trichodiscomas
- Familial multiple trichoepitheliomata
- Familial Nasal Acilia
- Familial Neurocardiogenic Syncope
- Familial non-Hodgkin lymphoma
- Familial Non-Immune Hyperthyroidism
- Familial Opposable Triphalangeal Thumbs Duplication
- Familial osteodysplasia
- Familial Periodic Paralysis
- Familial Platelet Disorder with Associated Myeloid Malignancy
- Familial Porencephaly
- Familial porphyria cutanea tarda
- Familial progressive cardiac conduction defect
- Familial psoriasis
- Familial pulmonary fibrosis
- Familial Renal Cell Carcinoma
- Familial renal glucosuria
- Familial renal hypouricemia
- Familial restrictive cardiomyopathy 1
- Familial restrictive cardiomyopathy 3
- Familial Spastic Paraparesis
- Familial symmetric lipomatosis
- Familial thoracic aortic aneurysm and dissection
- Familial Treacher Collins syndrome
- Familial Tremor
- Familial vasovagal syncope
- Familial venous malformations
- Familial ventricular tachycardia
- Familial Wilms Tumor 2
- Familial x-linked hypophosphatemic vitamin D refractory rickets
- FAMMM syndrome
- Fanconi Anemia
- Fanconi anemia, complementation group B
- Fanconi Bickel Syndrome
- Fanconi Renotubular Syndrome
- Fanconi renotubular syndrome 2
- Fanconi syndrome
- FAP
- Farber's Disease
- Farber's lipogranulomatosis
- Farmer's Lung
- Fascioliasis
- Fasting plasma glucose level quantitative trait locus 5
- Fatal Birth Anomalies
- Fatal Familial Insomnia
- Fatty Oxidation Disorders
- Faulk Epstein Jones Syndrome
- Faye-Petersen Ward Carey Syndrome
- Fazio Londe Syndrome
- Fealty Syndrome
- Febrile Infection-Related Epilepsy Syndrome
- Febrile seizures
- Febrile seizures, familial, 11
- Febrile seizures, familial, 4
- Febrile Ulceronecrotic Mucha-Habermann Disease
- Fechtner syndrome
- Feigenbaum Bergeron Richardson Syndrome
- Feigenbaum Bergeron Syndrome
- Feingold syndrome
- Feingold syndrome 2
- Feingold Trainer Syndrome
- Felty's Syndrome
- Female Sexual Dysfunction
- Femoral Facial Syndrome
- Femur Bifid with Monodactylous Ectrodactyly
- Femur Fibula Ulna Syndrome
- Fetal Akinesia Deformation Sequence
- Fetal Akinesia Syndrome X-Linked
- Fetal Alcohol Spectrum Disorders
- Fetal Alcohol Syndrome (FAS)
- Fetal Aminopterin Syndrome
- Fetal and Neonatal Alloimmune Thrombocytopenia
- Fetal Brain Disruption Sequence
- Fetal hemoglobin quantitative trait locus 1
- Fetal hemoglobin quantitative trait locus 6
- Fetal Hydantoin Syndrome
- Fetal Indomethacin Syndrome
- Fetal Left Ventricular Aneurysm
- Fetal Macrosomia
- Fetal Methyl Mercury Syndrome
- Fetal ovarian cyst
- Fetal Retinoid Syndrome
- Fetal Valproate Syndrome
- Fetal Warfarin Syndrome