Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 1951 to 2000 of 11113 Records | Page: 40 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_European-American
- obsolete_Ewing family tumor
- obsolete_Ewing sarcoma
- obsolete_Exanthema Subitum
- obsolete_External ear
- obsolete_Extrahepatic Bile Duct Adenosquamous Carcinoma
- obsolete_Extrahepatic Bile Duct Squamous Cell Carcinoma
- obsolete_Extramammary Paget Disease
- obsolete_Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
- obsolete_FADD-related immunodeficiency
- obsolete_FASTKD2-related infantile mitochondrial encephalomyopathy
- obsolete_FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
- obsolete_FGFR2-related bent bone dysplasia
- obsolete_FGFR3-related chondrodysplasia
- obsolete_FISSEQ
- obsolete_FLOTCH syndrome
- obsolete_FRAXE intellectual disability
- obsolete_FRAXF syndrome
- obsolete_Fabry disease
- obsolete_Fallopian Tube Carcinoma
- obsolete_Fallopian Tube Carcinosarcoma
- obsolete_Fallopian Tube Serous Adenocarcinoma
- obsolete_Familial amyloid polyneuropathy
- obsolete_Familial aortic dissection
- obsolete_Familial capillary hemangioma
- obsolete_Familial dementia, British type
- obsolete_Familial dementia, Danish type
- obsolete_Familial hyperaldosteronism
- obsolete_Familial hyperaldosteronism type I
- obsolete_Familial hypercholanemia
- obsolete_Familial hypospadias
- obsolete_Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
- obsolete_Familial papillary renal cell carcinoma
- obsolete_Familial partial lipodystrophy associated with PLIN1 mutations
- obsolete_Familial partial lipodystrophy associated with PPARG mutations
- obsolete_Familial platelet syndrome with predisposition to acute myelogenous leukemia
- obsolete_Familial porphyria cutanea tarda
- obsolete_Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement
- obsolete_Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
- obsolete_Familial renal amyloidosis due to Apolipoprotein AII variant
- obsolete_Familial symmetric lipomatosis
- obsolete_Familial temporal epilepsy
- obsolete_Familial vascular leukoencephalopathy
- obsolete_Fanconi anemia
- obsolete_Farber lipogranulomatosis
- obsolete_Fascioliasis
- obsolete_Fatal infantile cytochrome C oxidase deficiency
- obsolete_Feingold syndrome
- obsolete_Feingold syndrome type 1
- obsolete_Feingold syndrome type 2
