Cystinuria
Cystinuria Cystinuria [[Image:{{{Image}}}|190px|center|]] {{{Caption}}} ICD-10 ... MedlinePlus {{{MedlinePlus}}} eMedicine {{{eMedicineSubj}}}/{{{eMedicineTopic}}} DiseasesDB {{{DiseasesDB}}} Cystinuria is an inherited autosomal recessive disorder and ... in the kidneys, ureter, and bladder. Causes Cystinuria is characterized by the inadequate reabsorption of ... dogs are at an increased risk to cystinuria, compared with other breeds of dogs. ...
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List of diseases starting with C
... aorta Cystin transport, protein defect of Cystinosis Cystinuria Cystinuria-lysinuria Cytochrome C oxidase deficiency Cytomegalic inclusion ...
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List codes CIM-10   (translated from French)
... E72.0) Disorders of amino-acid transport Cystinuria Cystinosis (E72.1) Disorders of sulfur-bearing ...
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List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders
... 0) Disturbances of amino-acid transport Cystinosis Cystinuria Hartnup disease (270.1) Phenylketonuria (PKU) (270 ...
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ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases
... metabolism (E720) Disorders of amino-acid transport Cystinuria Cystinosis Hartnup disease (E721) Disorders of sulfur ...
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Hartnup disease
... dermatitis, diarrhea and dementia. See also Cystinosis Cystinuria External links OMIM 234500 eMedicine University of ...
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Cystinosis
... 219750 - Adult nonnephropathic See also Hartnup disease Cystinuria Reference Genetics Home Reference External links eMedicine ...
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Penicillamine
... accumulated copper and elimination through urine. In cystinuria, a hereditary disorder featuring increased cystine excretion ...
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Archibald Garrod
... Garrod expanded his metabolic studies to cover cystinuria, pentosuria, and albinism. During the First World ...
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User:LinkBot/suggestions/Amino acid
... notably E. Coli and Yeast, to ... In Cystinuria, can backlink amino acids: ...nd bladder. The ...
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