Mondo Disease Ontology
1099 terms(s) returned
Term Type: Class | Record: 951 to 1000 of 1099 Records | Page: 20 of 22, First Previous Next Last | Show Records Per Page |
- ductal eccrine adenocarcinoma
- dumping syndrome
- duodenal adenocarcinoma
- duodenal atresia
- duodenal atresia tetralogy of fallot
- duodenal disorder
- duodenal gastrin-producing neuroendocrine tumor
- duodenal neuroendocrine neoplasm
- duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
- duodenal obstruction
- duodenal somatostatinoma
- duodenal ulcer
- duodenal ulcer due to antral G-cell hyperfunction
- duodenal ulcer, hyperpepsinogenemic 1
- duodenal villous adenoma
- duodenitis
- duodenogastric reflux
- duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery
- duodenum cancer
- duplication of leg mirror foot
- duplication of the pituitary gland
- duplication of the thumb unilateral biphalangeal
- duplication of urethra
- duplication/inversion 15q11
- dupont sellier chochillon syndrome
- dural sinus malformation
- dwarfism bluish sclerae
- dwarfism deafness retinitis pigmentosa
- dwarfism lethal type advanced bone age
- dwarfism thin bones multiple fractures
- dwarfism with stiff joints and ocular abnormalities
- dwarfism with tall vertebrae
- dwarfism, Levi type
- dwarfism, familial, with muscle spasms
- dwarfism, intellectual disability, and eye abnormality
- dwarfism, low-birth-weight type, with unresponsiveness to growth hormone
- dwarfism, proportionate, with hip dislocation
- dysautonomia
- dysautonomia, dog
- dysautonomia, domestic cat
- dysautonomia, horse
- dysautonomia, llama
- dysautonomia, non-human animal
- dysautonomia, rabbit
- dysautonomia-like disorder
- dysbaric osteonecrosis
- dyscalculia
- dyschondrosteosis-nephritis syndrome
- dyschromatosis symmetrica hereditaria
- dyschromatosis universalis hereditaria