Mondo Disease Ontology
4428 terms(s) returned
| Term Type: | Record: 51 to 100 of 4428 Records | Page: 2 of 89, First Previous Next Last | Show Records Per Page |
- obsolete 15q24 microdeletion syndrome
- obsolete 17-hydroxysteroid dehydrogenase deficiency
- obsolete 2-hydroxyglutaric aciduria
- obsolete 2q31.1 microduplication syndrome
- obsolete 3-Methylcrotonyl-CoA carboxylase deficiency
- obsolete 3-methylglutaconic aciduria, type VIII
- obsolete 46 XY gonadal dysgenesis
- obsolete 46,XX disorder of gonadal development
- obsolete 46,XX disorder of sex development induced by androgens excess
- obsolete 46,XX disorder of sex development induced by endogenous maternal-derived androgen
- obsolete 46,XX disorder of sex development induced by exogenous maternal-derived androgen
- obsolete 46,XX disorder of sex development induced by fetal androgens excess
- obsolete 46,XX disorder of sex development induced by fetoplacental androgens excess
- obsolete 46,XX disorder of sex development induced by maternal-derived androgen
- obsolete 46,XX sex reversal
- obsolete 46,XX sex reversal 1
- obsolete 46,XY disorder of gonadal development
- obsolete 46,XY disorder of sex development due to a cholesterol synthesis defect
- obsolete 46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue
- obsolete 46,XY disorder of sex development due to a testosterone synthesis defect
- obsolete 46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect
- obsolete 46,XY disorder of sex development due to impaired androgen production
- obsolete 46,XY disorder of sex development due to isolated 17,20-lyase deficiency
- obsolete 46,XY disorder of sex development due to testicular steroidogenesis defect
- obsolete 46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors
- obsolete 46,XY disorder of sex development of endocrine origin
- obsolete 46,XY disorder of sex development of gynecological interest
- obsolete 46,XY disorder of sexual development due to dihydrotestosterone backdoor pathway biosynthesis defect
- obsolete ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor
- obsolete AP4-related intellectual disability and spastic paraplegia
- obsolete ARC syndrome
- obsolete ARX-related encephalopathy-brain malformation spectrum
- obsolete ARX-related epileptic encephalopathy
- obsolete ATP13A2-related parkinsonism
- obsolete AVSD 1
- obsolete Abderhalden-Kaufmann-Lignac syndrome
- obsolete Acanthamoeba keratitis
- obsolete Adams-Oliver syndrome
- obsolete Addison disease
- obsolete Adie syndrome
- obsolete African tick typhus
- obsolete Alagille syndrome
- obsolete Alpers syndrome
- obsolete Alzheimer disease 15
- obsolete Alzheimer disease 5
- obsolete Alzheimer disease, susceptibility to, mitochondrial
- obsolete American trypanosomiasis
- obsolete Amish infantile epilepsy syndrome
- obsolete Amish infantile epilepsy syndrome
- obsolete Angelman syndrome chromosome region
