colobomata
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coloboma — col·o·bo·ma (kŏl ə bōʹmə) n. pl. col·o·bo·ma·ta ( mə tə) An anomaly of the eye, usually a developmental defect, that often results in some loss of vision. [New Latin colobōma, from Greek kolobōma, part removed in mutilation, from koloboun, to… … Universalium
Wolf–Hirschhorn syndrome — Wolf Hirschhorn syndrome Classification and external resources ICD 10 Q93.3 ICD 9 758.3 … Wikipedia
Monosomy 14 — Monosomy is a form of aneuploidy with the presence of only one chromosome (instead of the typical two in humans) from a pair, which affects chromosome 14. Fetuses with monosomy 14 are not viable.[1] Only mosaic cases exist and these usually… … Wikipedia
COACH — Canadian Organization for the Advancement of Computers in Health; cerebellar vermis hypoplasia/aplasia oligophrenia congenital ataxia ocular colobomata hepatic fibrosis [syndrome] … Medical dictionary
síndrome del coloboma macular hereditario — Eng. Syndrome of the hereditary ocular colobomata Ver síndrome de Sorsby … Diccionario de oftalmología
COACH — • Canadian Organization for the Advancement of Computers in Health; • cerebellar vermis hypoplasia/aplasia oligophrenia congenital ataxia ocular colobomata hepatic fibrosis [syndrome] … Dictionary of medical acronyms & abbreviations
