- polydystrophy
- 다발이상증
English-Korean animal medical dictionary. 2013.
polydystrophy
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polydystrophy — A condition characterized by the presence of many congenital anomalies. [poly + dystrophy] pseudo Hurler p. SYN: mucolipidosis III. * * * poly·dys·tro·phy (pol″e disґtrə fe) dystrophy of several tissues or structures at the same time.… … Medical dictionary
Pseudo-Hurler polydystrophy — Classification and external resources ICD 10 E77.0 ICD 9 272.7 … Wikipedia
Pseudo-Hurler polydystrophy — A rare genetic disease that is passed on via an autosomal recessive gene. It is characterized by abnormal lysosomal enzyme transport in cells of mesenchymal origin, causing elevated lysosomal enzymes in body fluids and tissues. Diagnosis is by… … Medical dictionary
variant pseudo-Hurler polydystrophy — mucolipidosis III gamma … Medical dictionary
Mucolipidosis — Classification and external resources ICD 10 E77.0 E77.1 ICD 9 … Wikipedia
Glycoprotein — Not to be confused with peptidoglycan or proteoglycan. N linked protein glycosylation (N glycosylation of N glycans) at Asn residues (Asn x Ser/Thr motifs) in glycoproteins.[1] Glycoproteins are proteins that contain oligosaccharide chai … Wikipedia
Congenital disorder of glycosylation — Congenital disorders of glycosylation Classification and external resources ICD 10 E77.8 ICD 9 271.8 … Wikipedia
Sialidosis — Classification and external resources Sialic acid ICD 10 E77.1 OMIM … Wikipedia
Mannosidosis — is a deficiency in mannosidase, an enzyme.[1] There are two types: Alpha mannosidosis Beta mannosidosis See also Swainsonine References ^ MeSH Mannosidosis … Wikipedia
Glycoproteinosis — ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Glycoproteinosis (or glycoprotein storage disorders ) are lysosomal storage diseases affecting glycoproteins, resulting from defects in lysosomal function.Types* (E77.0)… … Wikipedia
Mucolipidosis type IV — Classification and external resources ICD 10 E75.1 OMIM 252650 DiseasesDB … Wikipedia
