Experimental Factor Ontology
386 terms(s) returned
Term Type: | Record: 151 to 200 of 386 Records | Page: 4 of 8, First Previous Next Last | Show Records Per Page |
- endomyometritis
- endophthalmitis
- endove syndrome, limb-brain type
- enhanced S-cone syndrome
- enlarged vestibular aqueduct syndrome
- enteritis
- enteropathy-associated T-cell lymphoma
- enthesitis
- entropion
- enuresis
- eosinophil disorder
- eosinophil peroxidase deficiency
- eosinophilic gastroenteritis
- eosinophilic gastrointestinal disease
- ependymal tumor of brain
- ependymal tumor of spinal cord
- ependymoblastoma
- epiblepharon
- epibulbar lipodermoid-preauricular appendage-polythelia syndrome
- epicardium cancer
- epicardium lipoma
- epidemic keratoconjunctivitis
- epidemic louse-borne typhus
- epidermal appendage tumor
- epidermal disease
- epidermal nevus syndrome
- epidermodysplasia verruciformis
- epidermodysplasia verruciformis, X-linked
- epidermolysis bullosa simplex
- epidermolysis bullosa simplex 1A, generalized severe
- epidermolysis bullosa simplex 1B, generalized intermediate
- epidermolysis bullosa simplex 1C, localized
- epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
- epidermolysis bullosa simplex 2A, generalized severe
- epidermolysis bullosa simplex 2B, generalized intermediate
- epidermolysis bullosa simplex 2C, localized
- epidermolysis bullosa simplex 2E, with migratory circinate erythema
- epidermolysis bullosa simplex 2F, with mottled pigmentation
- epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive
- epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
- epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive
- epidermolysis bullosa simplex 5B, with muscular dystrophy
- epidermolysis bullosa simplex 5C, with pyloric atresia
- epidermolysis bullosa simplex 6, generalized, with scarring and hair loss
- epidermolysis bullosa simplex 7, with nephropathy and deafness
- epidermolysis bullosa simplex due to plakophilin deficiency
- epidermolysis bullosa simplex superficialis
- epidermolysis bullosa simplex with anodontia/hypodontia
- epidermolysis bullosa simplex with nail dystrophy
- epidermolysis bullosa, junctional 2A, intermediate