- Autosomal dominant oculocutaneous albinism
- 常染色体显性遗传眼皮肤白化病
Medical Chinese dictionary (湘雅医学词典). 2013.
Medical Chinese dictionary (湘雅医学词典). 2013.
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
Albinism — Albino redirects here. For other uses, see Albino (disambiguation). Albinism Classification and external resources A black child with albinism ICD 10 … Wikipedia
Ocular albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 … Wikipedia
Ocular albinism type 1 — Classification and external resources ICD 10 E70.3 OMIM 300500 DiseasesDB … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
List of diseases (O) — A list of diseases in the English wikipedia.O Ob* O Doherty syndrome * O Donnell Pappas syndrome * Obesity * Obesophobia * Obsessive compulsive disorder * Obstructive asymmetric septal hypertrophy * Obstructive sleep apneaOcOcc Och* Occipital… … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Albinotisch — Klassifikation nach ICD 10 E70.3 Albinismus … Deutsch Wikipedia
Pigmentstoffarmer Mensch — Klassifikation nach ICD 10 E70.3 Albinismus … Deutsch Wikipedia
Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 … Wikipedia
Medical genetics of Jewish people — The medical genetics of Jewish people is the study, screening and treatment of genetic disorders that are more common in particular Jewish populations than in the population as a whole.[1] The genetics of Ashkenazi Jews have been particularly… … Wikipedia