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oc·u·lo·cu·ta·ne·ous (ok″u-lo-ku-taґne-əs) pertaining to or affecting both the eyes and the skin.Medical dictionary. 2011.
Oculocutaneous albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 … Wikipedia
Oculocutaneous 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 … Wikipedia
oculocutaneous 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… … Medical dictionary
tyrosinase-positive oculocutaneous albinism — oculocutaneous a. type 2 … Medical dictionary
yellow mutant oculocutaneous albinism — oculocutaneous a. type 1b … Medical dictionary
oculocutaneous melanosis — oculodermal melanosis nevus of Ota … Medical dictionary
temperature-sensitive oculocutaneous albinism — a phenotypic variant of oculocutaneous albinism type 1b in which activity of the abnormal tyrosinase ceases above 35°C, so that the hair on warmer areas of the body is light and becomes progressively darker on the cooler areas (the extremities) … Medical dictionary
tyrosinase-negative oculocutaneous albinism — (ATN) oculocutaneous a. type 1a … Medical dictionary
OCA2 — Oculocutaneous albinism II Identifiers Symbols OCA2; BEY; BEY1; BEY2; BOCA; D15S12; EYCL; EYCL2; EYCL3; HCL3; P; PED; SHEP1 External IDs … Wikipedia
OCA1 — Oculocutaneous Albinism Type 1 (OCA1) is the gene associated with albinism, an autosomal recessive disorder. Albinism occurs when something causes the OCA1 gene to function improperly. The locus of gene OCA1 may be written 11q1.4 q2.1 , meaning… … Wikipedia
