(albinism)
31Oculocutaneous albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 …
32Ocular albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 …
33Persecution of people with albinism — A person with albinism Part of …
34Oculocutaneous albinism type I — Classification and external resources OMIM 203100 Oculocutaneous Albinism Type I or –Type 1A (OCA1A)[1] is an autosomal recessive skin disease associated with albi …
35autosomal recessive ocular albinism — a type of albinism formerly believed to be an autosomal recessive form of ocular albinism but now considered to belong within the phenotypes of oculocutaneous albinism types 1 and 2 …
36ocular albinism — (OA) X linked albinism that affects primarily the eyes, with pigment of the hair and skin being normal or only slightly diluted. It is characterized by reduced visual acuity, retinal hypopigmentation, the presence of macromelanosomes in the eyes …
37oculocutaneous albinism — (OCA) albinism characterized by partial or total absence of melanin from the melanocytes of the skin, hair, and eyes, with additional ocular defects including hypoplastic fovea, photophobia, nystagmus, and decreased visual acuity. There are a… …
38brown albinism — brown oculocutaneous albinism a phenotypic variant of oculocutaneous albinism type 2 seen in persons from normally dark skinned groups; pigmentation is deficient but not absent and photophobia is less severe than in other tyrosinase positive… …
39Nettleship-Falls ocular albinism — Net·tle·ship Falls ocular albinism (netґəl ship fawlzґ) [Edward Nettleship, English ophthalmologist and dermatologist, 1845–1913; Harold Francis Falls, American ophthalmologist and geneticist, 1909–2006] see under albinism …
40Nettleship-Falls ocular albinism — Nettleship Falls type ocular albinism ocular a. type 1 …
