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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Other Metabolic Disorders And Immunity Disorders 270-279 > Disorders Of Amino-Acid Transport And Metabolism 270.* > 2008 ICD-9-CM Diagnosis 270.0 Disturbances of amino-acid transport A disorder of amino acid transport characterized by the childhood (or rarely adult) onset of photosensitive dermatitis and intermittent neurologic symptoms. Ataxia, personality changes, migraine headaches, and photophobia may occur periodically. The disorder results from impaired sodium-dependent transport of neutral amino acids across the brush border membrane of the small intestine and renal tubular epithelium. (From Menkes, Textbook of Child Neurology, 5th ed, pp59-60) An autosomal recessive hereditary disorder characterized by defective transportation of cystine across the lysosomal membranes and systemic deposition of cystine crystals in the body. It is associated with slight increase of the plasma cystine, cystinuria, aminoaciduria, glycosuria, polyuria, hypophosphatemia, rickets, and renal tubular dysfunction. --2004 An inherited abnormality of renal tubular transport of dibasic amino acids leading to massive urinary excretion of cystine, lysine, arginine, and ornithine. Constellation of clinical and laboratory manifestations produced by generalized proximal tubular insufficiency in the presence of normal, or nearly normal, glomerular filtration. Lysosomal storage disorders of unknown molecular defect, characterized by widespread deposition of cystine crystals in reticuloendothelial cells. (From Dorland, 27th ed) 270.0 is a specific code that can be used to specify a diagnosis 270.0 contains 49 index entries View the ICD-9-CM Volume 1 270.* hierarchy 270.0 also known as: Cystinosis Cystinuria Fanconi (-de Toni) (-Debré) syndrome Glycinuria (renal) Hartnup disease Index entries containing 270.0: Abderhalden-Kaufmann-Lignac syndrome (cystinosis) 270.0 Beta-mercaptolactate-cysteine disulfiduria 270.0 Blue diaper syndrome 270.0 Cystinosis (malignant) 270.0 Cystinuria 270.0 Deficiency, deficient sulfite oxidase 270.0 de Toni-Fanconi syndrome (cystinosis) 270.0 Diathesis cystine (familial) 270.0 Disease, diseased - see also Syndrome cystine storage (with renal sclerosis) 270.0 H 270.0 Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0 Hartnup (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0 Lignac's (cystinosis) 270.0 Disorder - see also Disease amino acid (metabolic) (see also Disturbance, metabolism, amino acid) 270.9 cystinosis 270.0 cystinuria 270.0 glycinuria 270.0 renal transport NEC 270.0 transport NEC 270.0 renal 270.0 metabolism NEC 277.9 cystine storage 270.0 cystinuria 270.0 Disturbance - see also Disease amino acid (metabolic) (see also Disorder, amino acid) 270.9 transport 270.0 metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9 amino acid (see also Disorder, amino acid) 270.9 transport 270.0 Disulfiduria, beta-mercaptolactate-cysteine 270.0 Dwarf, dwarfism 259.4 nephrotic-glycosuric, with hypophosphatemic rickets 270.0 Fanconi (-de Toni) (-Debré) syndrome (cystinosis) 270.0 Glycinuria (renal) (with ketosis) 270.0 Hart's disease or syndrome (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0 Hartnup disease (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0 H disease 270.0 Hyperaminoaciduria 270.9 cystine 270.0 glycine 270.0 renal (types I, II, III) 270.0 Lignac's disease (cystinosis) 270.0 Lignac (-de Toni) (-Fanconi) (-Debré) syndrome (cystinosis) 270.0 Lignac (-Fanconi) syndrome (cystinosis) 270.0 Pellagra-cerebellar-ataxia-renal aminoaciduria syndrome 270.0 Rickets (active) (acute) (adolescent) (adult) (chest wall) (congenital) (current) (infantile) (intestinal) 268.0 hypophosphatemic with nephrotic-glycosuric dwarfism 270.0 Sclerosis, sclerotic renal 587 with cystine storage disease 270.0 Stone(s) - see also Calculus cystine 270.0 Syndrome - see also Disease blue diaper 270.0 de Toni-Fanconi (-Debre) (cystinosis) 270.0 Fanconi (-de Toni) (-Debré) (cystinosis) 270.0 Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0 Lignac (-de Toni) (-Fanconi) (-Debré) (cystinosis) 270.0 pellagra-cerebellar ataxia-renal aminoaciduria 270.0 Toni-Fanconi (cystinosis) 270.0 Thesaurismosis cystine 270.0 Toni-Fanconi syndrome (cystinosis) 270.0