Mondo Disease Ontology
2525 terms(s) returned
| Term Type: | Record: 1251 to 1300 of 2525 Records | Page: 26 of 51, First Previous Next Last | Show Records Per Page |
- epidemic louse-borne typhus
- epidemic pleurodynia
- epidermal Langerhans cell
- epidermal appendage tumor
- epidermal cell
- epidermal cell differentiation
- epidermal disease
- epidermal keratinocyte
- epidermal melanocyte
- epidermal nevus syndrome
- epidermal nevus vitamin D resistant rickets
- epidermis development
- epidermis gland
- epidermis suprabasal layer
- epidermitis, exudative, of swine
- epidermodysplasia verruciformis
- epidermodysplasia verruciformis, X-linked
- epidermodysplasia verruciformis, susceptibility to
- epidermodysplasia verruciformis, susceptibility to, 1
- epidermodysplasia verruciformis, susceptibility to, 2
- epidermodysplasia verruciformis, susceptibility to, 3
- epidermodysplasia verruciformis, susceptibility to, 4
- epidermodysplasia verruciformis, susceptibility to, 5
- epidermoid cysts
- epidermolysis bullosa
- epidermolysis bullosa dystrophica
- epidermolysis bullosa dystrophica Neurotrophica
- epidermolysis bullosa dystrophica with subcorneal cleavage
- 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
