Mondo Disease Ontology
1872 terms(s) returned
| Term Type: | Record: 651 to 700 of 1872 Records | Page: 14 of 38, First Previous Next Last | Show Records Per Page |
- fallot complex-intellectual disability-growth delay syndrome
- falx cerebri
- familial Alzheimer disease
- familial Alzheimer-like prion disease
- familial Dupuytren contracture
- familial Mediterranean fever
- familial Mediterranean fever, autosomal dominant
- familial abdominal aortic aneurysm
- familial acanthosis nigricans
- familial acne inversa
- familial acute necrotizing encephalopathy
- familial acute respiratory distress syndrome, ANLN-related, dog
- familial adenomatous polyposis 1
- familial adenomatous polyposis 2
- familial adenomatous polyposis 3
- familial adenomatous polyposis 4
- familial adenomatous polyposis due to 5q22.2 microdeletion
- familial adenomatous polyposis, APC-related, dog
- familial adenomatous polyposis, non-human animal
- familial adenomatous polyposis, pig
- familial adrenal hypoplasia with absent pituitary luteinizing hormone
- familial amyloid neuropathy
- familial amyotrophic lateral sclerosis
- familial anetoderma
- familial angiolipomatosis
- familial antiphospholipid syndrome
- familial apolipoprotein C-II deficiency
- familial apolipoprotein gene cluster deletion syndrome
- 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 capillaro-venous leptomeningeal angiomatosis
- familial cardiomyopathy
- familial caudal dysgenesis
- familial cavitary optic disk anomaly
- familial cervical artery dissection
- familial chilblain lupus
- familial chronic myelocytic leukemia-like syndrome
- 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
