Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q461486> ?p ?o }
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- Q461486 abstract "In anatomy, heterochromia (ancient Greek: ἕτερος, héteros, different + χρώμα, chróma, color) is a difference in coloration, usually of the iris but also of hair or skin. Heterochromia is a result of the relative excess or lack of melanin (a pigment). It may be inherited, or caused by genetic mosaicism, chimerism, disease, or injury.Heterochromia of the eye (heterochromia iridis or heterochromia iridum) is of three kinds. In complete heterochromia, one iris is a different color from the other. In sectoral heterochromia, part of one iris is a different color from its remainder and finally in "central heterochromia" there are spikes of different colours radiating from the pupil.Though multiple causes have been posited, the scientific consensus is that inbreeding is the primary reason behind heterochromia. This is due to mutation of the genes that determine melanin distribution at the 8-HTP pathway, which usually only become corrupted due to chromosomal homogeneity.Eye color, specifically the color of the irises, is determined primarily by the concentration and distribution of melanin. The affected eye may be hyperpigmented (hyperchromic) or hypopigmented (hypochromic). In humans, usually, an excess of melanin indicates hyperplasia of the iris tissues, whereas a lack of melanin indicates hypoplasia.".
- Q461486 icd10 "Q13.2,H20.8,L67.1".
- Q461486 icd9 "364.53".
- Q461486 omim "142500".
- Q461486 thumbnail Heterochromia.jpg?width=300.
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