Mondo Disease Ontology
2502 terms(s) returned
| Term Type: | Record: 2001 to 2050 of 2502 Records | Page: 41 of 51, First Previous Next Last | Show Records Per Page |
- hyperhomocysteinemia
- hyperhomocysteinemia, dog
- hyperhomocysteinemia, non-human animal
- hyperimmunoglobulin G1(A1) syndrome
- hyperimmunoglobulin syndrome
- hyperimmunoglobulinemia D with periodic fever
- hyperinsulinemic hypoglycemia
- hyperinsulinemic hypoglycemia with polycystic kidney disease
- hyperinsulinemic hypoglycemia, familial, 1
- hyperinsulinemic hypoglycemia, familial, 2
- hyperinsulinemic hypoglycemia, familial, 4
- hyperinsulinemic hypoglycemia, familial, 8
- hyperinsulinism
- hyperinsulinism due to HNF1A deficiency
- hyperinsulinism due to HNF4A deficiency
- hyperinsulinism due to INSR deficiency
- hyperinsulinism due to UCP2 deficiency
- hyperinsulinism due to glucokinase deficiency
- hyperinsulinism-hyperammonemia syndrome
- hyperkalemic periodic paralysis
- hyperkalemic periodic paralysis, horse
- hyperkalemic periodic paralysis, non-human animal
- hyperkalemic renal tubular acidosis
- hyperkeratosis lenticularis perstans
- hyperkeratosis, non-human animal
- hyperkeratosis-hyperpigmentation syndrome
- hyperkinesis, dog
- hyperkinesis, non-human animal
- hyperleucine-Isoleucinemia
- hyperlexia
- hyperlipidemia
- hyperlipidemia due to hepatic triglyceride lipase deficiency
- hyperlipidemia, combined, 1
- hyperlipidemia, combined, 2
- hyperlipidemia, familial combined, LPL related
- hyperlipidemia, non-human animal
- hyperlipoproteinemia
- hyperlipoproteinemia type 3
- 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
- hypermanganesemia with dystonia
- hypermanganesemia with dystonia 2
- hypermature cataract
- hypermetabolism due to defect in mitochondria
- hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2
