Mondo Disease Ontology
2689 terms(s) returned
| Term Type: | Record: 1351 to 1400 of 2689 Records | Page: 28 of 54, First Previous Next Last | Show Records Per Page |
- 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
- epidermoid cysts, non-human animal
- 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
- epidermolysis bullosa simplex, KRT14-related, domestic cat
- epidermolysis bullosa simplex, KRT5-related, cattle
- epidermolysis bullosa simplex, KRT5-related, dog
- epidermolysis bullosa simplex, PLEC-related, dog
- epidermolysis bullosa simplex, cattle
- epidermolysis bullosa simplex, dog
- epidermolysis bullosa simplex, non-human animal
- epidermolysis bullosa simplex, water buffalo
- epidermolysis bullosa with congenital localized absence of skin and deformity of nails
