2007 ICD-9-CM Diagnosis Code 270.2
Other disturbances of aromatic amino-acid metabolism
- Short description: AROM AMIN-ACID METAB NEC.
- ICD-9-CM 270.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 270.2 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).
- You are viewing the 2007 version of ICD-9-CM 270.2.
- More recent version(s) of ICD-9-CM 270.2: 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
270.2 converts approximately to:
- 2015/16 ICD-10-CM E70.21 Tyrosinemia
Or:
- 2015/16 ICD-10-CM E70.29 Other disorders of tyrosine metabolism
Or:
- 2015/16 ICD-10-CM E70.30 Albinism, unspecified
Or:
- 2015/16 ICD-10-CM E70.5 Disorders of tryptophan metabolism
Or:
- 2015/16 ICD-10-CM E70.8 Other disorders of aromatic amino-acid metabolism
Approximate Synonyms
- 4-Hydroxyphenylpyruvate dioxygenase deficiency
- Aland eye disease and ocular albinism
- Albinism
- Albinism w hematologic abnormality
- Albinism with hematologic disorder
- Albinism-deafness syndrome of Tietz
- Albinoidism
- Albinotic fundus
- Alcaptonuric ochronosis
- Alkaptonuria
- Aromatic amino acid metabolism disorder
- Aromatic amino acid, metabolism disturbances
- Autosomal dominant oculocutaneous albinism
- Autosomal recessive ocular albinism
- Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
- Brown oculocutaneous albinism
- Disorder of aromatic amino acid metabolism
- 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
- Hermansky-Pudlak syndrome
- Homogentisate 1,2-dioxygenase deficiency
- Hydroxykynureninuria
- Hypertyrosinemia
- Hypertyrosinemia, Richner Hanhart type
- Hypertyrosinemia, Richner-Hanhart type
- Hypopigmentation-immunodeficiency disease
- Indicanuria
- Klein-Waardenberg's syndrome
- Kynureninase deficiency
- Minimal pigment oculocutaneous albinism
- Ochronosis
- Ochronosis due to homogentisate 1,2-dioxygenase deficiency
- Ochronosis due to hydroquinone
- Ochronotic arthritis
- Ocular albinism
- Ocular albinism (eye condition)
- 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
- Tryptophan metabolism disorder
- Tryptophanuria
- Tyrosinase negative oculocutaneous albinism
- Tyrosinase positive oculocutaneous albinism
- Tyrosinase-negative oculocutaneous albinism
- Tyrosinase-positive oculocutaneous albinism
- Tyrosine metabolism disorder
- Tyrosinemia
- Tyrosinemia type 1
- Tyrosinemia type 2
- Tyrosinemia type 3
- Tyrosinemia type I
- Tyrosinemia type III
- Tyrosinemia, type 3
- Tyrosinosis
- Tyrosinuria
- Waardenburgs syndrome
- Waardenburg's syndrome
- Woolf's syndrome
- X linked ocular albinism
- Yellow mutant oculocutaneous albinism
- Ziprkowski-Margolis syndrome
270.2 Excludes
- vitamin B6-deficiency syndrome (266.1
)
Applies To
- Albinism
- Alkaptonuria
- Alkaptonuric ochronosis
- Disturbances of metabolism of tyrosine and tryptophan
- Homogentisic acid defects
- Hydroxykynureninuria
- Hypertyrosinemia
- Indicanuria
- Kynureninase defects
- Oasthouse urine disease
- Ochronosis
- Tyrosinosis
- Tyrosinuria
- Waardenburg syndrome
congenital 270.2
homogentisic acid 270.2
