Mondo Disease Ontology
1603 terms(s) returned
| Term Type: | Record: 701 to 750 of 1603 Records | Page: 15 of 33, First Previous Next Last | Show Records Per Page |
- familial hyperprolactinemia
- familial hyperreninemic hypoaldosteronism type 2
- familial hyperthyroidism due to mutations in TSH receptor
- familial hypertrophic cardiomyopathy
- familial hypertryptophanemia
- familial hypoaldosteronism
- familial hypobetalipoproteinemia 1
- familial hypobetalipoproteinemia 2
- familial hypocalciuric hypercalcemia
- familial hypocalciuric hypercalcemia 1
- familial hypocalciuric hypercalcemia 2
- familial hypocalciuric hypercalcemia 3
- familial hypodysfibrinogenemia
- familial hypofibrinogenemia
- familial hypoparathyroidism
- familial idiopathic dilatation of the right atrium
- familial idiopathic inflammatory myopathy
- familial idiopathic steroid-resistant nephrotic syndrome
- familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
- familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
- familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
- familial idiopathic torsion dystonia
- familial infantile bilateral striatal necrosis
- familial infantile myoclonic epilepsy
- familial intestinal malrotation-facial anomalies syndrome
- familial intrahepatic cholestasis
- familial isolated arrhythmogenic right ventricular dysplasia
- familial isolated arrhythmogenic ventricular dysplasia, biventricular form
- familial isolated arrhythmogenic ventricular dysplasia, left dominant form
- familial isolated arrhythmogenic ventricular dysplasia, right dominant form
- familial isolated clinodactyly of fingers
- familial isolated congenital asplenia
- familial isolated deficiency of vitamin E
- familial isolated dilated cardiomyopathy
- familial isolated hyperparathyroidism
- familial isolated hypoparathyroidism due to agenesis of parathyroid gland
- familial isolated hypoparathyroidism due to impaired PTH secretion
- familial isolated pituitary adenoma
- familial isolated trichomegaly
- familial juvenile hypertrophy of the breast
- familial juvenile hyperuricemic nephropathy
- familial juvenile hyperuricemic nephropathy type 1
- familial juvenile hyperuricemic nephropathy type 2
- familial keratoacanthoma
- familial lipochrome histiocytosis
- familial lipoprotein lipase deficiency
- familial long QT syndrome
- familial male-limited precocious puberty
- familial median cleft of the upper and lower lips
- familial medullary thyroid carcinoma
