Mondo Disease Ontology
3935 terms(s) returned
| Term Type: | Record: 3701 to 3750 of 3935 Records | Page: 75 of 79, First Previous Next Last | Show Records Per Page |
- myeloid/lymphoid neoplasm associated with JAK2 rearrangement
- myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
- myelolymphatic insufficiency
- myelomeningocele
- myeloperoxidase deficiency
- myeloperoxidase deficiency, dog
- myeloperoxidase deficiency, non-human animal
- myelophthisic anemia
- myeloproliferative disease, autosomal recessive
- myeloproliferative disorder, chronic, with eosinophilia
- myeloproliferative neoplasm
- myeloproliferative neoplasm, unclassifiable
- myeloschisis
- myiasis
- myoblast
- myocardial disorder
- myocardial endocrine cell
- myocardial endocrine cell of atrium
- myocardial endocrine cell of interventricular septum
- myocardial infarction
- myocardial infarction, susceptibility to
- myocardial infarction, susceptibility to, 2
- myocardial ischemia
- myocardial layer
- myocardial rupture
- myocardial stunning
- myocarditis
- myocardium
- myocardium cancer
- myocardium of anterior wall of left ventricle
- myocardium of anterior wall of right ventricle
- myocardium of atrium
- myocardium of ventricle
- myocardium trabecular layer
- myoclonic cerebellar dyssynergia
- myoclonic dystonia 11
- myoclonic dystonia 15
- myoclonic dystonia 26
- myoclonic encephalopathy in non-progressive disorder
- myoclonic epilepsy
- myoclonic epilepsy in infancy
- myoclonic epilepsy in non-progressive encephalopathies
- myoclonic epilepsy of Lafora 1
- myoclonic epilepsy of Lafora 2
- myoclonic epilepsy, Hartung type
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
- myoclonic epilepsy, juvenile, 2
- myoclonic epilepsy, juvenile, susceptibility to, 1
- myoclonic epilepsy, juvenile, susceptibility to, 3
- myoclonic epilepsy, juvenile, susceptibility to, 4
