Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (references) |
Source: compiled by the editor from various references; see credits. | |
Hexadecimal (or equivalents, 770AD-1900s) (references)41 44 52 45 4E 41 4C 48 59 50 45 52 50 4C 41 53 49 41 2C 43 4F 4E 47 45 4E 49 54 41 4C |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01000001 01000100 01010010 01000101 01001110 01000001 01001100 00100000 01001000 01011001 01010000 01000101 01010010 01010000 01001100 01000001 01010011 01001001 01000001 00101100 00100000 01000011 01001111 01001110 01000111 01000101 01001110 01001001 01010100 01000001 01001100 |
HTML Code (1990) (references)A D R E N A L   H Y P E R P L A S I A ,   C O N G E N I T A L |
ISO 10646 (1991-1993) (references)0041 0044 0052 0045 004E 0041 004C 0048 0059 0050 0045 0052 0050 004C 0041 0053 0049 0041 002C 0043 004F 004E 0047 0045 004E 0049 0054 0041 004C |
Encryption (beginner's substitution cypher): (references)353852394835462425950395250463553433514237494841394843543546 |
| 1. Orthography 2. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
