Experimental Factor Ontology
926 terms(s) returned
Term Type: | Record: 201 to 250 of 926 Records | Page: 5 of 19, First Previous Next Last | Show Records Per Page |
- malignant tenosynovial giant cell tumor
- malignant teratoma
- malignant teratoma of mediastinum
- malignant teratoma of testis
- malignant testicular Leydig cell tumor
- malignant testicular germ cell tumor
- malignant triton tumor
- malignant tumor of adrenal cortex
- malignant tumor of extrahepatic bile duct
- malignant tumor of floor of mouth
- malignant tumor of meninges
- malignant tumor of minor salivary gland
- malignant tumor of nasopharynx
- malignant tumor of neck
- malignant tumor of palpebral epidermis
- malignant tumor of parathyroid gland
- malignant type AB thymoma
- malignant vaginal mixed epithelial and mesenchymal neoplasm
- malonic aciduria
- malt worker's lung
- mammary Paget disease
- mammary-digital-nail syndrome
- mandibular hypoplasia-deafness-progeroid syndrome
- mandibuloacral dysplasia
- mandibuloacral dysplasia progeroid syndrome
- mandibuloacral dysplasia with type A lipodystrophy
- mandibuloacral dysplasia with type B lipodystrophy
- mandibulofacial dysostosis
- mandibulofacial dysostosis with alopecia
- mandibulofacial dysostosis with mental deficiency
- mandibulofacial dysostosis-macroblepharon-macrostomia syndrome
- mandibulofacial dysostosis-microcephaly syndrome
- mannose-binding lectin deficiency
- maple syrup urine disease
- maple syrup urine disease type 1A
- maple syrup urine disease type 1B
- marcothrombocytopenia with mitral valve insufficiency
- marfanoid habitus-autosomal recessive intellectual disability syndrome
- marfanoid habitus-inguinal hernia-advanced bone age syndrome
- mast syndrome
- mastocytoma
- maternal 14q32.2 hypermethylation syndrome
- maternal 14q32.2 microdeletion syndrome
- maternal phenylketonuria
- maternal riboflavin deficiency
- maternal uniparental disomy of chromosome 1
- maternal uniparental disomy of chromosome 13
- maternal uniparental disomy of chromosome 14
- maternal uniparental disomy of chromosome 16
- maternal uniparental disomy of chromosome 2