Mondo Disease Ontology
2764 terms(s) returned
| Term Type: | Record: 2251 to 2300 of 2764 Records | Page: 46 of 56, First Previous Next Last | Show Records Per Page |
- hyperlipoproteinemia type V
- hyperlipoproteinemia, type 1D
- hyperlipoproteinemia, type II, and deafness
- hyperlucent lung
- hyperlysinemia
- hyperlysinemia due to defect in lysine transport into mitochondria
- hyperlysinuria with hyperammonemia
- hypermagnesemia, non-human animal
- hypermanganesemia with dystonia
- hypermanganesemia with dystonia 2
- hypermature cataract
- hypermetabolism due to defect in mitochondria
- hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2
- hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
- hypermobility of coccyx
- hypermobility spectrum disorder
- hypermobility syndrome
- hypernatremia, non-human animal
- hyperoestrogenism, non-human animal
- hyperopia
- hyperopia, high
- hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, horse
- hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, non-human animal
- hyperosmolar non-ketotic diabetic syndrome, non-human animal
- hyperosmolar nonketotic diabetes mellitus, domestic cat
- hyperosmolar nonketotic diabetes mellitus, non-human animal
- hyperostosis
- hyperostosis corticalis generalisata
- hyperostosis cranialis interna
- hyperostosis, non-human animal
- hyperostosis, pig
- hyperoxaluria, koala
- hyperparathyroidism
- hyperparathyroidism 1
- hyperparathyroidism 2 with jaw tumors
- hyperparathyroidism 3
- hyperparathyroidism 4
- hyperparathyroidism, dog
- hyperparathyroidism, domestic cat
- hyperparathyroidism, horse
- hyperparathyroidism, neonatal self-limited primary, with hypercalciuria
- hyperparathyroidism, non-human animal
- hyperparathyroidism, primary, caused by water clear cell hyperplasia
- hyperparathyroidism, transient neonatal
- hyperphagia leading to hepatic steatosis, non-human animal
- hyperphagia leading to hepatic steatosis, pig
- hyperphalangy
- hyperphalangy, bilateral
- hyperphalangy, unilateral
- hyperphenylalaninemia due to DNAJC12 deficiency
