Experimental Factor Ontology
70 terms(s) returned
| Term Type: | Record: 1 to 50 of 70 Records | Page: 1 of 2, First Previous Next Last | Show Records Per Page |
- FTH1-related iron overload
- Facial dysmorphism - immunodeficiency - livedo - short stature
- Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation
- Facial dysmorphism - shawl scrotum - joint laxity
- Facioscapulohumeral dystrophy
- Fallot complex - intellectual disability - growth delay
- Familial hyperprolactinemia
- Familial LCAT deficiency
- Familial Scheuermann disease
- Familial adenomatous polyposis
- Familial advanced sleep-phase syndrome
- Familial afibrinogenemia
- Familial amyloidosis, Finnish type
- Familial benign chronic pemphigus
- Familial cerebral saccular aneurysm
- Familial cervical artery dissections
- Familial chondromalacia patellae
- Familial cold urticaria
- Familial cortical myoclonus
- Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
- Familial drusen
- Familial dysautonomia
- Familial dyskinesia and facial myokymia
- Familial esophageal achalasia
- Familial exudative vitreoretinopathy
- Familial gastric cancer
- Familial hemophagocytic lymphohistiocytosis
- Familial hypocalciuric hypercalcemia type 1
- Familial hypocalciuric hypercalcemia type 2
- Familial hypocalciuric hypercalcemia type 3
- Familial intestinal malrotation - facial anomalies
- Familial isolated hypoparathyroidism
- Familial multinodular goiter
- Familial ocular anterior segment mesenchymal dysgenesis
- Familial osteochondritis dissecans
- Familial paroxysmal ataxia
- Familial partial lipodystrophy due to AKT2 mutations
- Familial partial lipodystrophy, Köbberling type
- Familial progressive cardiac conduction defect
- Familial prostate cancer
- Familial renal amyloidosis
- Familial renal amyloidosis due to Apolipoprotein AI variant
- Familial renal amyloidosis due to fibrinogen A alpha-chain variant
- Familial renal amyloidosis due to lysozyme variant
- Familial retinoblastoma
- Familial short QT syndrome
- Familial transthyretin-related amyloidosis
- Fatal infantile lactic acidosis with methylmalonic aciduria
- Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3
- Fatal multiple mitochondrial dysfunction syndrome
