Experimental Factor Ontology
421 terms(s) returned
Term Type: | Record: 101 to 150 of 421 Records | Page: 3 of 9, First Previous Next Last | Show Records Per Page |
- fallopian tube transitional cell carcinoma
- fallot complex-intellectual disability-growth delay syndrome
- familial Alzheimer disease
- familial Dupuytren contracture
- familial Mediterranean fever
- familial abdominal aortic aneurysm
- familial acanthosis nigricans
- familial acne inversa
- familial acute necrotizing encephalopathy
- familial adenomatous polyposis 1
- familial adenomatous polyposis 2
- familial adenomatous polyposis 4
- familial adenomatous polyposis due to 5q22.2 microdeletion
- familial adrenal hypoplasia with absent pituitary luteinizing hormone
- familial anetoderma
- familial angiolipomatosis
- familial apolipoprotein C-II deficiency
- familial atrial fibrillation
- familial atrial myxoma
- familial atrioventricular septal defect
- familial atypical multiple mole melanoma syndrome
- familial avascular necrosis of femoral head
- familial benign copper deficiency
- familial benign flecked retina
- familial bent bone dysplasia syndrome
- familial bicuspid aortic valve
- familial caudal dysgenesis
- familial cavitary optic disk anomaly
- familial cervical artery dissection
- familial chilblain lupus
- familial chylomicronemia syndrome
- familial clubfoot due to 17q23.1q23.2 microduplication
- familial clubfoot due to 5q31 microdeletion
- familial clubfoot due to PITX1 point mutation
- familial clubfoot with or without associated lower limb anomalies
- familial cold autoinflammatory syndrome
- familial cold autoinflammatory syndrome 1
- familial cold autoinflammatory syndrome 2
- familial cold autoinflammatory syndrome 3
- familial cold autoinflammatory syndrome 4
- familial colorectal cancer
- familial congenital mirror movements
- familial congenital nasolacrimal duct obstruction
- familial congenital palsy of trochlear nerve
- familial cutaneous collagenoma
- familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
- familial cylindromatosis
- familial cystic renal disease
- familial digital arthropathy-brachydactyly
- familial dilated cardiomyopathy