Mondo Disease Ontology
3933 terms(s) returned
| Term Type: | Record: 3301 to 3350 of 3933 Records | Page: 67 of 79, First Previous Next Last | Show Records Per Page |
- multicentric Castleman disease
- multicentric Castleman disease, susceptibility to
- multicentric carpo-tarsal osteolysis with or without nephropathy
- multicentric osteolysis, nodulosis, and arthropathy
- multicentric osteolysis-nodulosis-arthropathy spectrum
- multicentric papillary thyroid carcinoma
- multicentric reticulohistiocytosis
- multiciliated
- multiciliated columnar cell of tracheobronchial tree
- multiciliated epithelial cell
- multiciliated epithelial cell of the bronchus
- multicomponent meal (us cfr)
- multicystic dysplastic kidney
- multidrug-resistant tuberculosis
- multifocal atrial tachycardia
- multifocal choroiditis
- multifocal dystonia
- multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
- multifocal motor neuropathy
- multifocal osteogenic sarcoma
- multifocal pattern dystrophy simulating fundus flavimaculatus
- multifocal retinopathy 1, BEST1-related, dog
- multifocal retinopathy 2, BEST1-related, dog
- multifocal retinopathy 3, BEST1-related, dog
- multifocal symmetrical necrotizing encephalomyelopathy, Angus cattle
- multifocal symmetrical necrotizing encephalomyelopathy, Simmental cattle
- multifocal tuberculosis
- multilaminar epithelium
- multilocular clear cell renal cell carcinoma
- multiloculated renal cyst
- multiminicore myopathy
- multinodular and vacuolating neuronal tumor
- multinodular goiter
- multinodular goiter-cystic kidney-polydactyly syndrome
- multinucleate
- multinucleate cell
- multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
- multiple acyl-CoA dehydrogenase deficiency
- multiple acyl-CoA dehydrogenase deficiency, domestic cat
- multiple acyl-CoA dehydrogenase deficiency, horse
- multiple acyl-CoA dehydrogenase deficiency, mild type
- multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
- multiple acyl-coa dehydrogenase deficiency, non-human animal
- multiple autoimmune diseases syndrome, dog
- multiple autoimmune diseases syndrome, non-human animal
- multiple benign circumferential skin creases on limbs
- multiple benign circumferential skin creases on limbs 1
- multiple carboxylase deficiency
- multiple congenital anomalies due to 14q32.2 imprinting defect
- multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
