Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from mucopolysaccharidosis I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. (references) |
Source: compiled by the editor from various references; see credits. | |
Hexadecimal (or equivalents, 770AD-1900s) (references)4D 55 43 4F 50 4F 4C 59 53 41 43 43 48 41 52 49 44 4F 53 49 53 49 49 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01001101 01010101 01000011 01001111 01010000 01001111 01001100 01011001 01010011 01000001 01000011 01000011 01001000 01000001 01010010 01001001 01000100 01001111 01010011 01001001 01010011 00100000 01001001 01001001 |
HTML Code (1990) (references)M U C O P O L Y S A C C H A R I D O S I S   I I |
ISO 10646 (1991-1993) (references)004D 0055 0043 004F 0050 004F 004C 0059 0053 0041 0043 0043 0048 0041 0052 0049 0044 004F 0053 0049 0053 0049 0049 |
Encryption (beginner's substitution cypher): (references)47553749504946595335373742355243384953435324343 |
| 1. Orthography 2. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
