270.2 - Other Disturbances Of Aromatic Amino-acid Metabolism
The ICD 9 Code for Other disturbances of aromatic amino-acid metabolism is listed as 270.2.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 270.2 |
| Long Description: | Other disturbances of aromatic amino-acid metabolism |
| Short Description: | Arom amin-acid metab NEC |
| Chapter: | Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders |
| Block: | Other Metabolic Disorders And Immunity Disorders (270-279) |
| Related Descriptions: |
4-Hydroxyphenylpyruvate dioxygenase deficiency
Aland eye disease and ocular albinism Albinism Albinism-deafness syndrome of Tietz Albinoidism Albinotic fundus Alkaptonuria Autosomal dominant oculocutaneous albinism Autosomal recessive ocular albinism Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Brown oculocutaneous albinism Disorder of tryptophan metabolism Disorder of tyrosine metabolism Exogenous ochronosis Fumarylacetoacetase deficiency, acute type Fumarylacetoacetase deficiency, chronic type Glutaryl-CoA oxidase deficiency Hereditary hypertyrosinemia Hermansky-Pudlak syndrome Homogentisate 1,2-dioxygenase deficiency Hydroxykynureninuria Hypertyrosinemia Hypertyrosinemia, Richner-Hanhart type Hypopigmentation-immunodeficiency disease Indicanuria Klein-Waardenberg's syndrome Kynureninase deficiency Minimal pigment oculocutaneous albinism Ochronosis due to homogentisate 1,2-dioxygenase deficiency Ochronosis due to hydroquinone Ochronotic arthritis Ocular albinism Ocular albinism, type I Ocular albinism, type II Ocular albinism-lentigines-deafness syndrome Oculocutaneous albinism Oculocutaneous albinoidism Partial albinism Punctate oculocutaneous albinoidism Rufous albinism Temperature-sensitive oculocutaneous albinism Tryptophanuria Tyrosinase-negative oculocutaneous albinism Tyrosinase-positive oculocutaneous albinism Tyrosinemia Tyrosinemia type I Tyrosinemia type III Tyrosinosis Tyrosinuria Woolf's syndrome Yellow mutant oculocutaneous albinism Ziprkowski-Margolis syndrome |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | E70.21 - Tyrosinemia (approximate) |
| ICD-10-CM Code: | E70.29 - Other disorders of tyrosine metabolism (approximate) |
| ICD-10-CM Code: | E70.30 - Albinism, unspecified (approximate) |
| ICD-10-CM Code: | E70.5 - Disorders of tryptophan metabolism (approximate) |
| ICD-10-CM Code: | E70.8 - Other disorders of aromatic amino-acid metabolism (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 270.2: | |
| 270.0 - Disturbances of amino-acid transport | |
| 270.1 - Phenylketonuria [PKU] | |
| 270.3 - Disturbances of branched-chain amino-acid metabolism | |
| 270.4 - Disturbances of sulphur-bearing amino-acid metabolism | |
| 270.5 - Disturbances of histidine metabolism | |
| 270.6 - Disorders of urea cycle metabolism | |
| 270.7 - Other disturbances of straight-chain amino-acid metabolism | |
| 270.8 - Other specified disorders of amino-acid metabolism | |
| 270.9 - Unspecified disorder of amino-acid metabolism | |