Achromasia Biography

| ICD9 = | ICDO = | OMIM = 203100 | OMIM_mult = , , , , , , , , , , , , , , , , , , , , | MedlinePlus = 001479 | eMedicineSubj = derm | eMedicineTopic = 12 | MeshID = | }}Albinism (from Latin albus, "white"; see extended etymology) is a form of hypopigmentary congenital disorder, characterized by a partial (in hypomelanism, also known as hypomelanosis) or total (amelanism or amelanosis) lack of melanin pigment in the eyes, skin and hair (or more rarely the eyes alone). Albinism results from inheritance of recessive genes. The condition is known to affect mammals (including humans), fish, birds, reptiles, and amphibians. While the most common term for an organism affected by albinism is "albino" (noun and adjective), the word is sometimes used in derogatory ways towards people; more neutral terms are "albinistic" (adjective) and "person with albinism" (noun). Additional clinical adjectives sometimes used to refer to animals a

Source: http://en.wikipedia.org/wiki/Achromasia
 

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