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ICD-10-CM-2017 Diagnosis Codes Overview
ICD-10-CM-2017 > E00-E89 > E70-E88 > E72
E70-E88
Metabolic disorders
Excl1.:
androgen insensitivity syndrome (icd E34.5 Androgen insensitivity syndromeE34.5-)
congenital adrenal hyperplasia (icd E25.0 Congenital adrenogenital disorders associated with enzyme deficiencyE25.0)
Ehlers-Danlos syndrome (icd Q79.6 Ehlers-Danlos syndromeQ79.6)
hemolytic anemias attributable to enzyme disorders (icd D55 Anemia due to enzyme disordersD55.-)
Marfan's syndrome (icd Q87.4 Marfan's syndromeQ87.4)
5-alpha-reductase deficiency (icd E29.1 Testicular hypofunctionE29.1)
E72

Other disorders of amino-acid metabolism

Excl1.:
disorders of:
aromatic amino-acid metabolism (icd E70 Disorders of aromatic amino-acid metabolismE70.-)
branched-chain amino-acid metabolism (icd E71.0 Maple-syrup-urine diseaseE71.0-icd E71.2 Disorder of branched-chain amino-acid metabolism, unspecifiedE71.2)
fatty-acid metabolism (icd E71.3 Disorders of fatty-acid metabolismE71.3)
purine and pyrimidine metabolism (icd E79 Disorders of purine and pyrimidine metabolismE79.-)
gout (icd M1A Chronic goutM1A.-, icd M10 GoutM10.-)
E72.0

Disorders of amino-acid transport

Excl1.:
disorders of tryptophan metabolism (icd E70.5 Disorders of tryptophan metabolismE70.5)
E72.00
Disorders of amino-acid transport, unspecified
E72.01
Cystinuria
E72.02
Hartnup's disease
E72.03
Lowe's syndrome
Use add'l
code for associated glaucoma (icd H42 Glaucoma in diseases classified elsewhereH42)
E72.04
Cystinosis
Info:
Fanconi (-de Toni) (-Debré) syndrome with cystinosis
Excl1.:
Fanconi (-de Toni) (-Debré) syndrome without cystinosis (icd E72.09 Other disorders of amino-acid transportE72.09)
E72.09
Other disorders of amino-acid transport
Info:
Fanconi (-de Toni) (-Debré) syndrome, unspecified
E72.1

Disorders of sulfur-bearing amino-acid metabolism

Excl1.:
cystinosis (icd E72.04 CystinosisE72.04)
cystinuria (icd E72.01 CystinuriaE72.01)
transcobalamin II deficiency (icd D51.2 Transcobalamin II deficiencyD51.2)
E72.10
Disorders of sulfur-bearing amino-acid metabolism, unspecified
E72.11
Homocystinuria
Info:
Cystathionine synthase deficiency
E72.12
Methylenetetrahydrofolate reductase deficiency
E72.19
Other disorders of sulfur-bearing amino-acid metabolism
Info:
Cystathioninuria
Methioninemia
Sulfite oxidase deficiency
E72.2

Disorders of urea cycle metabolism

Excl1.:
disorders of ornithine metabolism (icd E72.4 Disorders of ornithine metabolismE72.4)
E72.20
Disorder of urea cycle metabolism, unspecified
Info:
Hyperammonemia
Excl1.:
hyperammonemia-hyperornithinemia-homocitrullinemia syndrome icd E72.4 Disorders of ornithine metabolismE72.4
transient hyperammonemia of newborn (icd P74.6 Transitory hyperammonemia of newbornP74.6)
E72.21
Argininemia
E72.22
Arginosuccinic aciduria
E72.23
Citrullinemia
E72.29
Other disorders of urea cycle metabolism
E72.3
Disorders of lysine and hydroxylysine metabolism
Info:
Glutaric aciduria NOS
Glutaric aciduria (type I)
Hydroxylysinemia
Hyperlysinemia
Excl1.:
glutaric aciduria type II (icd E71.313 Glutaric aciduria type IIE71.313)
Refsum's disease (icd G60.1 Refsum's diseaseG60.1)
Zellweger syndrome (icd E71.510 Zellweger syndromeE71.510)
E72.4
Disorders of ornithine metabolism
Info:
Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome
Ornithinemia (types I, II)
Ornithine transcarbamylase deficiency
Excl1.:
hereditary choroidal dystrophy (icd H31.2 Hereditary choroidal dystrophyH31.2-)
E72.5

Disorders of glycine metabolism

E72.50
Disorder of glycine metabolism, unspecified
E72.51
Non-ketotic hyperglycinemia
E72.52
Trimethylaminuria
E72.53
Hyperoxaluria
Info:
Oxalosis
Oxaluria
E72.59
Other disorders of glycine metabolism
Info:
D-glycericacidemia
Hyperhydroxyprolinemia
Hyperprolinemia (types I, II)
Sarcosinemia
E72.8
Other specified disorders of amino-acid metabolism
Info:
Disorders of beta-amino-acid metabolism
Disorders of gamma-glutamyl cycle
E72.9
Disorder of amino-acid metabolism, unspecified


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