Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. (references) |
Source: compiled by the editor from various references; see credits. | |
| Language | Translations for "EPIDERMOLYSIS BULLOSA DYSTROPHICA"; alternative meanings/domain in parentheses. | ||||
French | syndrome de Nicolas-Moutot-Charlet (epidermolysis bullosa dystrophica ulcerovegetans). (various references) | ||||
German | Epidermolysis bullosa dystrophica ulcerovegetans (epidermolysis bullosa dystrophica ulcerovegetans), Nicolas-Moutot-Charlet Syndrom (epidermolysis bullosa dystrophica ulcerovegetans). (various references) | ||||
Pig Latin | epidermolysisay ullosabay ystrophicaday | ||||
Hexadecimal (or equivalents, 770AD-1900s) (references)45 50 49 44 45 52 4D 4F 4C 59 53 49 53 42 55 4C 4C 4F 53 41 44 59 53 54 52 4F 50 48 49 43 41 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01000101 01010000 01001001 01000100 01000101 01010010 01001101 01001111 01001100 01011001 01010011 01001001 01010011 00100000 01000010 01010101 01001100 01001100 01001111 01010011 01000001 00100000 01000100 01011001 01010011 01010100 01010010 01001111 01010000 01001000 01001001 01000011 01000001 |
HTML Code (1990) (references)E P I D E R M O L Y S I S   B U L L O S A   D Y S T R O P H I C A |
ISO 10646 (1991-1993) (references)0045 0050 0049 0044 0045 0052 004D 004F 004C 0059 0053 0049 0053 0042 0055 004C 004C 004F 0053 0041 0044 0059 0053 0054 0052 004F 0050 0048 0049 0043 0041 |
Encryption (beginner's substitution cypher): (references)3950433839524749465953435323655464649533523859535452495042433735 |
| 1. Translations: Modern 2. Orthography 3. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
