Departments of Anesthesiology and Biostatistics | University of Michigan

ICD mappings

ICD code Type Description Phenome
C88.0 ICD10CM Waldenstrom macroglobulinemia MGI
D47.2 ICD10CM Monoclonal gammopathy MGI
D89.0 ICD10CM Polyclonal hypergammaglobulinemia MGI
D89.1 ICD10CM Cryoglobulinemia MGI
E70 ICD10CM Disorders of aromatic amino-acid metabolism MGI
E70.0 ICD10CM Classical phenylketonuria MGI
E70.1 ICD10CM Other hyperphenylalaninemias MGI
E70.2 ICD10CM Disorders of tyrosine metabolism MGI
E70.20 ICD10CM Disorder of tyrosine metabolism, unspecified MGI
E70.21 ICD10CM Tyrosinemia MGI
E70.29 ICD10CM Other disorders of tyrosine metabolism MGI
E70.3 ICD10CM Albinism MGI
E70.30 ICD10CM Albinism, unspecified MGI
E70.31 ICD10CM Ocular albinism MGI
E70.310 ICD10CM X-linked ocular albinism MGI
E70.311 ICD10CM Autosomal recessive ocular albinism MGI
E70.318 ICD10CM Other ocular albinism MGI
E70.319 ICD10CM Ocular albinism, unspecified MGI
E70.32 ICD10CM Oculocutaneous albinism MGI
E70.320 ICD10CM Tyrosinase negative oculocutaneous albinism MGI
E70.321 ICD10CM Tyrosinase positive oculocutaneous albinism MGI
E70.328 ICD10CM Other oculocutaneous albinism MGI
E70.329 ICD10CM Oculocutaneous albinism, unspecified MGI
E70.33 ICD10CM Albinism with hematologic abnormality MGI
E70.330 ICD10CM Chediak-Higashi syndrome MGI
E70.331 ICD10CM Hermansky-Pudlak syndrome MGI
E70.338 ICD10CM Other albinism with hematologic abnormality MGI
E70.339 ICD10CM Albinism with hematologic abnormality, unspecified MGI
E70.39 ICD10CM Other specified albinism MGI
E70.4 ICD10CM Disorders of histidine metabolism MGI
E70.40 ICD10CM Disorders of histidine metabolism, unspecified MGI
E70.41 ICD10CM Histidinemia MGI
E70.49 ICD10CM Other disorders of histidine metabolism MGI
E70.5 ICD10CM Disorders of tryptophan metabolism MGI
E70.8 ICD10CM Other disorders of aromatic amino-acid metabolism MGI
E70.9 ICD10CM Disorder of aromatic amino-acid metabolism, unspecified MGI
E71.0 ICD10CM Maple-syrup-urine disease MGI
E71.110 ICD10CM Isovaleric acidemia MGI
E71.111 ICD10CM 3-methylglutaconic aciduria MGI
E71.118 ICD10CM Other branched-chain organic acidurias MGI
E71.120 ICD10CM Methylmalonic acidemia MGI
E71.121 ICD10CM Propionic acidemia MGI
E71.128 ICD10CM Other disorders of propionate metabolism MGI
E71.19 ICD10CM Other disorders of branched-chain amino-acid metabolism MGI
E71.2 ICD10CM Disorder of branched-chain amino-acid metabolism, unspecified MGI
E72.0 ICD10CM Disorders of amino-acid transport MGI
E72.00 ICD10CM Disorders of amino-acid transport, unspecified MGI
E72.01 ICD10CM Cystinuria MGI
E72.02 ICD10CM Hartnup's disease MGI
E72.03 ICD10CM Lowe's syndrome MGI
E72.04 ICD10CM Cystinosis MGI
E72.09 ICD10CM Other disorders of amino-acid transport MGI
E72.1 ICD10CM Disorders of sulfur-bearing amino-acid metabolism MGI
E72.10 ICD10CM Disorders of sulfur-bearing amino-acid metabolism, unspecified MGI
E72.11 ICD10CM Homocystinuria MGI
E72.12 ICD10CM Methylenetetrahydrofolate reductase deficiency MGI
E72.19 ICD10CM Other disorders of sulfur-bearing amino-acid metabolism MGI
E72.2 ICD10CM Disorders of urea cycle metabolism MGI
E72.20 ICD10CM Disorder of urea cycle metabolism, unspecified MGI
E72.21 ICD10CM Argininemia MGI
E72.22 ICD10CM Arginosuccinic aciduria MGI
E72.23 ICD10CM Citrullinemia MGI
E72.29 ICD10CM Other disorders of urea cycle metabolism MGI
E72.3 ICD10CM Disorders of lysine and hydroxylysine metabolism MGI
E72.4 ICD10CM Disorders of ornithine metabolism MGI
E72.5 ICD10CM Disorders of glycine metabolism MGI
E72.50 ICD10CM Disorder of glycine metabolism, unspecified MGI
E72.51 ICD10CM Non-ketotic hyperglycinemia MGI
E72.52 ICD10CM Trimethylaminuria MGI
E72.53 ICD10CM Primary hyperoxaluria MGI
E72.59 ICD10CM Other disorders of glycine metabolism MGI
E72.8 ICD10CM Other specified disorders of amino-acid metabolism MGI
E72.9 ICD10CM Disorder of amino-acid metabolism, unspecified MGI
E88.01 ICD10CM Alpha-1-antitrypsin deficiency MGI
E88.09 ICD10CM Other disorders of plasma-protein metabolism, not elsewhere classified MGI
270.0 ICD9CM Disturbances of amino-acid transport MGI
270.1 ICD9CM Phenylketonuria [PKU] MGI
270.2 ICD9CM Other disturbances of aromatic amino-acid metabolism MGI
270.3 ICD9CM Disturbances of branched-chain amino-acid metabolism MGI
270.4 ICD9CM Disturbances of sulphur-bearing amino-acid metabolism MGI
270.5 ICD9CM Disturbances of histidine metabolism MGI
270.6 ICD9CM Disorders of urea cycle metabolism MGI
270.7 ICD9CM Other disturbances of straight-chain amino-acid metabolism MGI
270.8 ICD9CM Other specified disorders of amino-acid metabolism MGI
270.9 ICD9CM Unspecified disorder of amino-acid metabolism MGI
273.0 ICD9CM Polyclonal hypergammaglobulinemia MGI
273.1 ICD9CM Monoclonal paraproteinemia MGI
273.2 ICD9CM Other paraproteinemias MGI
273.3 ICD9CM Macroglobulinemia MGI
273.4 ICD9CM Alpha-1-antitrypsin deficiency MGI
273.8 ICD9CM Other disorders of plasma protein metabolism MGI
273.9 ICD9CM Unspecified disorder of plasma protein metabolism MGI
C88.0 ICD10 C88.0 Waldenstrom's macroglobulinaemia UKB
D47.2 ICD10 D47.2 Monoclonal gammopathy UKB
D89.0 ICD10 D89.0 Polyclonal hypergammaglobulinaemia UKB
D89.1 ICD10 D89.1 Cryoglobulinaemia UKB
E70.0 ICD10 E70.0 Classical phenylketonuria UKB
E70.1 ICD10 E70.1 Other hyperphenylalaninaemias UKB
E70.2 ICD10 E70.2 Disorders of tyrosine metabolism UKB
E70.3 ICD10 E70.3 Albinism UKB
E70.8 ICD10 E70.8 Other disorders of aromatic amino-acid metabolism UKB
E70.9 ICD10 E70.9 Disorder of aromatic amino-acid metabolism, unspecified UKB
E71.1 ICD10 E71.1 Other disorders of branched-chain amino-acid metabolism UKB
E72.0 ICD10 E72.0 Disorders of amino-acid transport UKB
E72.1 ICD10 E72.1 Disorders of sulphur-bearing amino-acid metabolism UKB
E72.2 ICD10 E72.2 Disorders of urea cycle metabolism UKB
E72.4 ICD10 E72.4 Disorders of ornithine metabolism UKB
E72.5 ICD10 E72.5 Disorders of glycine metabolism UKB
270 ICD9 270 Disorders of amino-acid transport and metabolism UKB

This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.

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