ICD-9-CM Diagnosis Code 270.0 : Disturbances of amino-acid transport

Home > 2015 ICD-9-CM Diagnosis Codes > 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-

2015 ICD-9-CM Diagnosis Code 270.0

Disturbances of amino-acid transport

2015
Billable Thru Sept 30/2015
Non-Billable On/After Oct 1/2015

ICD-9-CM 270.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 270.0 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).

Convert to ICD-10-CM: 270.0 converts approximately to:

2015/16 ICD-10-CM E72.00 Disorders of amino-acid transport, unspecified
Or:
2015/16 ICD-10-CM E72.01 Cystinuria
Or:
2015/16 ICD-10-CM E72.04 Cystinosis
Or:
2015/16 ICD-10-CM E72.09 Other disorders of amino-acid transport

Approximate Synonyms

3-methylcrotonyl glycinuria
Amino acid transport disorder
Cystinosis
Cystinuria
Cystinuria type 1
Cystinuria, type 1
Disorder of amino acid transport
Fanconi syndrome
Glycinuria, 3 methylcrotonyl
Hartnup disease
Methylcrotonyl-CoA carboxylase deficiency
Neutral 1 amino acid transport defect

Clinical Information

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
Constellation of clinical and laboratory manifestations produced by generalized proximal tubular insufficiency in the presence of normal, or nearly normal, glomerular filtration
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; results from impaired sodium-dependent transport of neutral amino acids across the brush border membrane of the small intestine and renal tubular epithelium
Inherited abnormality of renal tubular transport of dibasic amino acids leading to massive urinary excretion of cystine, lysine, arginine, and ornithine
Lysosomal storage disorders of unknown molecular defect, characterized by widespread deposition of cystine crystals in reticuloendothelial cells

Applies To

Cystinosis
Cystinuria
Fanconi (-de Toni) (-Debré) syndrome
Glycinuria (renal)
Hartnup disease

ICD-9-CM Volume 2 Index entries containing back-references to 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
  - albinism 270.2
  - alkaptonuria 270.2
  - argininosuccinicaciduria 270.6
  - beta-amino-isobutyricaciduria 277.2
  - cystathioninuria 270.4
  - cystinosis 270.0
  - cystinuria 270.0
  - glycinuria 270.0
  - homocystinuria 270.4
  - imidazole 270.5
  - maple syrup (urine) disease 270.3
  - neonatal, transitory 775.89
  - oasthouse urine disease 270.2
  - ochronosis 270.2
  - phenylketonuria 270.1
  - phenylpyruvic oligophrenia 270.1
  - purine NEC 277.2
  - pyrimidine NEC 277.2
  - renal transport NEC 270.0
  - specified type NEC 270.8
  - transport NEC 270.0
    - renal 270.0
  - xanthinuria 277.2
- metabolism NEC 277.9
  - with
    - abortion - see Abortion, by type, with metabolic disorder
    - ectopic pregnancy (see also categories 633.0-633.9) 639.4
    - molar pregnancy (see also categories 630-632) 639.4
  - alkaptonuria 270.2
  - amino acid (see also Disorder, amino acid) 270.9
    - specified type NEC 270.8
  - ammonia 270.6
  - arginine 270.6
  - argininosuccinic acid 270.6
  - basal 794.7
  - bilirubin 277.4
  - calcium 275.40
  - carbohydrate 271.9
    - specified type NEC 271.8
  - cholesterol 272.9
  - citrulline 270.6
  - copper 275.1
  - corticosteroid 255.2
  - cystine storage 270.0
  - cystinuria 270.0
  - fat 272.9
  - fatty acid oxidation 277.85
  - following
    - abortion 639.4
    - ectopic or molar pregnancy 639.4
  - fructosemia 271.2
  - fructosuria 271.2
  - fucosidosis 271.8
  - galactose-1-phosphate uridyl transferase 271.1
  - glutamine 270.7
  - glycine 270.7
  - glycogen storage NEC 271.0
    - hepatorenal 271.0
  - hemochromatosis (see also Hemochromatosis) 275.03
  - in labor and delivery 669.0
  - iron 275.09
  - lactose 271.3
  - lipid 272.9
    - specified type NEC 272.8
    - storage 272.7
  - lipoprotein - see also Hyperlipemia
    - deficiency (familial) 272.5
  - lysine 270.7
  - magnesium 275.2
  - mannosidosis 271.8
  - mineral 275.9
    - specified type NEC 275.8
  - mitochondrial 277.87
  - mucopolysaccharide 277.5
  - nitrogen 270.9
  - ornithine 270.6
  - oxalosis 271.8
  - pentosuria 271.8
  - phenylketonuria 270.1
  - phosphate 275.3
  - phosphorus 275.3
  - plasma protein 273.9
    - specified type NEC 273.8
  - porphyrin 277.1
  - purine 277.2
  - pyrimidine 277.2
  - serine 270.7
  - sodium 276.9
  - specified type NEC 277.89
  - steroid 255.2
  - threonine 270.7
  - urea cycle 270.6
  - xylose 271.8
Disturbance - see also Disease
- amino acid (metabolic) (see also Disorder, amino acid) 270.9
  - imidazole 270.5
  - maple syrup (urine) disease 270.3
  - transport 270.0
- metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9
  - with
    - abortion - see Abortion, by type, with metabolic disorder
    - ectopic pregnancy (see also categories 633.0-633.9) 639.4
    - molar pregnancy (see also categories 630-632) 639.4
  - amino acid (see also Disorder, amino acid) 270.9
    - aromatic NEC 270.2
    - branched-chain 270.3
    - specified type NEC 270.8
    - straight-chain NEC 270.7
    - sulfur-bearing 270.4
    - transport 270.0
  - ammonia 270.6
  - arginine 270.6
  - argininosuccinic acid 270.6
  - carbohydrate NEC 271.9
  - cholesterol 272.9
  - citrulline 270.6
  - cystathionine 270.4
  - fat 272.9
  - following
    - abortion 639.4
    - ectopic or molar pregnancy 639.4
  - general 277.9
    - carbohydrate 271.9
    - iron 275.09
    - phosphate 275.3
    - sodium 276.9
  - glutamine 270.7
  - glycine 270.7
  - histidine 270.5
  - homocystine 270.4
  - in labor or delivery 669.0
  - iron 275.09
  - isoleucine 270.3
  - leucine 270.3
  - lipoid 272.9
    - specified type NEC 272.8
  - lysine 270.7
  - methionine 270.4
  - neonatal, transitory 775.9
    - specified type NEC 775.89
  - nitrogen 788.99
  - ornithine 270.6
  - phosphate 275.3
  - phosphatides 272.7
  - serine 270.7
  - sodium NEC 276.9
  - threonine 270.7
  - tryptophan 270.2
  - tyrosine 270.2
  - urea cycle 270.6
  - valine 270.3
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
    - hypertension (see also Hypertension, kidney) 403.90
    - hypertensive heart disease (conditions classifiable to 402) (see also Hypertension, cardiorenal) 404.90
  - arteriolar (hyaline) (see also Hypertension, kidney) 403.90
    - hyperplastic (see also Hypertension, kidney) 403.90
Stone(s) - see also Calculus
- cystine 270.0
Syndrome - see also Disease
- blue
  - bloater 491.20
  - diaper 270.0
  - drum 381.02
  - sclera 756.51
  - toe 445.02
- 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

270

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270.1

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 270.0 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2015 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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