Experimental Factor Ontology
2682 terms(s) returned
| Term Type: | Record: 1901 to 1950 of 2682 Records | Page: 39 of 54, First Previous Next Last | Show Records Per Page |
- epidermal growth factor receptor substrate 15-like 1
- epidermal growth factor receptor substrate 15-like 1 level
- epidermal growth factor receptor substrate 15-like 1 (human)
- epidermal growth factor receptor substrate 15-like 1, initiator methionine removed form
- epidermal growth factor receptor substrate 15-like 1, initiator methionine removed form (human)
- epidermal growth factor receptor, signal peptide removed form
- epidermal growth factor receptor, signal peptide removed form (human)
- epidermal growth factor-like protein 6
- epidermal growth factor-like protein 6 (human)
- epidermal growth factor-like protein 7
- epidermal nevus syndrome
- epidermis suprabasal layer
- epidermodysplasia verruciformis
- epidermodysplasia verruciformis, X-linked
- epidermolysis bullosa
- epidermolysis bullosa dystrophica
- 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 5A, Ogna type
- 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
- epidermolysis bullosa, junctional 2B, severe
- epidermolysis bullosa, junctional 3A, intermediate
- epidermolysis bullosa, junctional 3B, severe
- epidermolysis bullosa, junctional 4, intermediate
- epidermolysis bullosa, junctional 5A, intermediate
- epidermolysis bullosa, junctional 6, with pyloric atresia
- epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
- epidermolytic acanthoma
- epidermolytic hyperkeratosis 2
- epidermolytic hyperkeratosis 2A, autosomal dominant
- epidermolytic hyperkeratosis 2B, autosomal recessive
