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
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
xanthinuria 277.2
- 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
- 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
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