Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | Autosomal recessive porphyria characterized by splenomegaly, photosensitivity, hemolytic anemia, and the appearance of red urine in early infancy. This condition results from increased synthesis of uroporphyrinogen I relative to uroporphyrinogen III in bone marrow normoblasts. (references) |
Source: compiled by the editor from various references; see credits. | |
| Language | Period | Translations |
| Latin | 500 BCE-Modern | porphyria cutanea tarda. (various references) |
| Source: compiled by the editor from various references. | ||
Hexadecimal (or equivalents, 770AD-1900s) (references)50 4F 52 50 48 59 52 49 41 2C 45 52 59 54 48 52 4F 50 4F 49 45 54 49 43 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01010000 01001111 01010010 01010000 01001000 01011001 01010010 01001001 01000001 00101100 00100000 01000101 01010010 01011001 01010100 01001000 01010010 01001111 01010000 01001111 01001001 01000101 01010100 01001001 01000011 |
HTML Code (1990) (references)P O R P H Y R I A ,   E R Y T H R O P O I E T I C |
ISO 10646 (1991-1993) (references)0050 004F 0052 0050 0048 0059 0052 0049 0041 002C 0045 0052 0059 0054 0048 0052 004F 0050 004F 0049 0045 0054 0049 0043 |
Encryption (beginner's substitution cypher): (references)5049525042595243351423952595442524950494339544337 |
| 1. Translations: Ancient 2. Orthography 3. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
