Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 1401 to 1450 of 11113 Records | Page: 29 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_Arabidopsis Growth Stage 6.50
- obsolete_Arabidopsis Growth Stage 8.00
- obsolete_Arabidopsis Growth Stage 9.70
- obsolete_Arbisopsis thaliana
- obsolete_Arbovirus Infections
- obsolete_Arenaviridae infectious disease
- obsolete_Arenavirus hemorrhagic fever
- obsolete_ArrayExpress experiment type
- obsolete_Arteritis
- obsolete_Arterivirus infectious disease
- obsolete_Ascaridida infectious disease
- obsolete_Ascending Colon Neuroendocrine Tumor G1
- obsolete_Ascher syndrome
- obsolete_Asian
- obsolete_Asian Indian
- obsolete_Asian/Pacific Islander
- obsolete_Askin Tumor
- obsolete_Asperger syndrome
- obsolete_Astley-Kendall dysplasia
- obsolete_Astroviridae infectious disease
- obsolete_Atkin-Flaitz syndrome
- obsolete_Atlas Quality Control type
- obsolete_Atlas experiment type
- obsolete_Atlas experiment type flag
- obsolete_Atrioventricular defect - blepharophimosis -radial defects
- obsolete_Atypical Carcinoid Tumor
- obsolete_Atypical Endometrial Hyperplasia
- obsolete_Atypical Lipomatous Tumor
- obsolete_Atypical Lobular Breast Hyperplasia
- obsolete_Atypical Mayer-Rokitansky-Küster-Hauser syndrome
- obsolete_Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
- obsolete_Autoimmune Hepatitis
- obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2
- obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
- obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2G
- obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2P
- obsolete_Autosomal dominant cervical dystonia
- obsolete_Autosomal dominant dopa-responsive dystonia
- obsolete_Autosomal dominant epilepsy with auditory features
- obsolete_Autosomal dominant focal dystonia, DYT7 type
- obsolete_Autosomal dominant limb-girdle muscular dystrophy type 1A
- obsolete_Autosomal dominant medullary cystic kidney disease without hyperuricemia
- obsolete_Autosomal dominant neovascular inflammatory vitreoretinopathy
- obsolete_Autosomal dominant non-syndromic sensorineural deafness type DFNA
- obsolete_Autosomal dominant polycystic kidney disease
- obsolete_Autosomal dominant spastic ataxia type 1
- obsolete_Autosomal recessive Charcot Marie Tooth disease type 2X
- obsolete_Autosomal recessive axonal Charcot-Marie-Tooth disease type 2
- obsolete_Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to KIAA0226 deficiency
- obsolete_Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency
