Human Disease Ontology
526 terms(s) returned
| Term Type: | Record: 251 to 300 of 526 Records | Page: 6 of 11, First Previous Next Last | Show Records Per Page |
- familial lipoprotein lipase deficiency
- familial male-limited precocious puberty
- familial medullary thyroid carcinoma
- familial melanoma
- familial meningioma
- familial multiple lipomatosis
- familial multiple nevi flammei
- familial nephrotic syndrome
- familial partial lipodystrophy
- familial partial lipodystrophy type 1
- familial partial lipodystrophy type 2
- familial partial lipodystrophy type 3
- familial partial lipodystrophy type 4
- familial partial lipodystrophy type 5
- familial partial lipodystrophy type 6
- familial periodic paralysis
- familial progressive hyperpigmentation with or without hypopigmentation
- familial renal glucosuria
- familial renal oncocytoma
- familial renal papillary carcinoma
- familial restrictive cardiomyopathy 1
- familial restrictive cardiomyopathy 2
- familial restrictive cardiomyopathy 3
- familial restrictive cardiomyopathy 6
- familial retinoblastoma
- familial temporal lobe epilepsy 1
- familial temporal lobe epilepsy 2
- familial temporal lobe epilepsy 3
- familial temporal lobe epilepsy 4
- familial temporal lobe epilepsy 5
- familial temporal lobe epilepsy 6
- familial temporal lobe epilepsy 7
- familial temporal lobe epilepsy 8
- familial thyroid dyshormonogenesis
- familial woolly hair syndrome
- farmer's lung
- fasciitis
- fascioliasis
- fascioloidiasis
- fasciolopsiasis
- fat necrosis of breast
- fatal familial insomnia
- fatigue
- favism
- feature_ablation
- feature_amplification
- feature_elongation
- feature_fusion
- feature_translocation
- feature_truncation
