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
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