Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 2501 to 2550 of 11113 Records | Page: 51 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_Mediterranean macrothrombocytopenia
- obsolete_Medullar aplasia
- obsolete_Medullomyoblastoma with Myogenic Differentiation
- obsolete_Meesmann corneal dystrophy
- obsolete_Megacystis-microcolon-intestinal hypoperistalsis syndrome
- obsolete_Melhem-Fahl syndrome
- obsolete_Melkersson-Rosenthal syndrome
- obsolete_Meniere disease
- obsolete_Menkes disease
- obsolete_Metanephric Adenoma
- obsolete_Methicillin-Resistant Staphylococcus Aureus Infection
- obsolete_Micrencephaly - corpus callosum agenesis - abnormal genitalia
- obsolete_Microcephaly - lymphedema - chorioretinopathy
- obsolete_Micropapillary Serous Carcinoma
- obsolete_Middle Ear Squamous Cell Carcinoma
- obsolete_Mietens syndrome
- obsolete_Mikati-Najjar-Sahli syndrome
- obsolete_Miller Fisher syndrome
- obsolete_Minor Salivary Gland Adenocarcinoma
- obsolete_Mixed Cell Uveal Melanoma
- obsolete_Mixed Lobular and Ductal Breast Carcinoma
- obsolete_Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma
- obsolete_Mixed Tumor of the Salivary Gland
- obsolete_Mixed Tumor of the Skin
- obsolete_Miyoshi myopathy
- obsolete_Mobius syndrome
- obsolete_Monieziasis
- obsolete_Monomelic amyotrophy
- obsolete_Mononegavirales infectious disease
- obsolete_Mononen-Karnes-Senac syndrome
- obsolete_Monosomy 13q14
- obsolete_Monosomy 18q
- obsolete_Morbillivirus infectious disease
- obsolete_Morgagni-Stewart-Morel syndrome
- obsolete_Morvan syndrome
- obsolete_Mowat-Wilson syndrome
- obsolete_Mowat-Wilson syndrome due to a ZEB2 point mutation
- obsolete_Mowat-Wilson syndrome due to monosomy 2q22
- obsolete_Moyamoya disease
- obsolete_Moyamoya disease
- obsolete_Moyamoya disease with early-onset achalasia
- obsolete_Moynahan syndrome
- obsolete_Mucinous Gastric Adenocarcinoma
- obsolete_Muckle-Wells syndrome
- obsolete_Mucolipidosis type II
- obsolete_Muenke syndrome
- obsolete_Muir-Torre syndrome
- obsolete_Multiple acyl-CoA dehydrogenation deficiency, mild type
- obsolete_Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
- obsolete_Multiple keratoacanthoma, Ferguson-Smith type
