Other disorders of metabolism
277
Endocrine/metabolic
Both
277-277.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| C96.5 | ICD10CM | Multifocal and unisystemic Langerhans-cell histiocytosis | MGI |
| C96.6 | ICD10CM | Unifocal Langerhans-cell histiocytosis | MGI |
| D81.3 | ICD10CM | Adenosine deaminase [ADA] deficiency | MGI |
| D81.5 | ICD10CM | Purine nucleoside phosphorylase [PNP] deficiency | MGI |
| E71.3 | ICD10CM | Disorders of fatty-acid metabolism | MGI |
| E71.30 | ICD10CM | Disorder of fatty-acid metabolism, unspecified | MGI |
| E71.31 | ICD10CM | Disorders of fatty-acid oxidation | MGI |
| E71.310 | ICD10CM | Long chain/very long chain acyl CoA dehydrogenase deficiency | MGI |
| E71.311 | ICD10CM | Medium chain acyl CoA dehydrogenase deficiency | MGI |
| E71.312 | ICD10CM | Short chain acyl CoA dehydrogenase deficiency | MGI |
| E71.313 | ICD10CM | Glutaric aciduria type II | MGI |
| E71.314 | ICD10CM | Muscle carnitine palmitoyltransferase deficiency | MGI |
| E71.318 | ICD10CM | Other disorders of fatty-acid oxidation | MGI |
| E71.32 | ICD10CM | Disorders of ketone metabolism | MGI |
| E71.39 | ICD10CM | Other disorders of fatty-acid metabolism | MGI |
| E71.4 | ICD10CM | Disorders of carnitine metabolism | MGI |
| E71.40 | ICD10CM | Disorder of carnitine metabolism, unspecified | MGI |
| E71.41 | ICD10CM | Primary carnitine deficiency | MGI |
| E71.42 | ICD10CM | Carnitine deficiency due to inborn errors of metabolism | MGI |
| E71.43 | ICD10CM | Iatrogenic carnitine deficiency | MGI |
| E71.44 | ICD10CM | Other secondary carnitine deficiency | MGI |
| E71.440 | ICD10CM | Ruvalcaba-Myhre-Smith syndrome | MGI |
| E71.448 | ICD10CM | Other secondary carnitine deficiency | MGI |
| E71.5 | ICD10CM | Peroxisomal disorders | MGI |
| E71.50 | ICD10CM | Peroxisomal disorder, unspecified | MGI |
| E71.51 | ICD10CM | Disorders of peroxisome biogenesis | MGI |
| E71.510 | ICD10CM | Zellweger syndrome | MGI |
| E71.511 | ICD10CM | Neonatal adrenoleukodystrophy | MGI |
| E71.518 | ICD10CM | Other disorders of peroxisome biogenesis | MGI |
| E71.52 | ICD10CM | X-linked adrenoleukodystrophy | MGI |
| E71.520 | ICD10CM | Childhood cerebral X-linked adrenoleukodystrophy | MGI |
| E71.521 | ICD10CM | Adolescent X-linked adrenoleukodystrophy | MGI |
| E71.522 | ICD10CM | Adrenomyeloneuropathy | MGI |
| E71.528 | ICD10CM | Other X-linked adrenoleukodystrophy | MGI |
| E71.529 | ICD10CM | X-linked adrenoleukodystrophy, unspecified type | MGI |
| E71.53 | ICD10CM | Other group 2 peroxisomal disorders | MGI |
| E71.54 | ICD10CM | Other peroxisomal disorders | MGI |
| E71.540 | ICD10CM | Rhizomelic chondrodysplasia punctata | MGI |
| E71.541 | ICD10CM | Zellweger-like syndrome | MGI |
| E71.542 | ICD10CM | Other group 3 peroxisomal disorders | MGI |
| E71.548 | ICD10CM | Other peroxisomal disorders | MGI |
| E75.21 | ICD10CM | Fabry (-Anderson) disease | MGI |
| E75.22 | ICD10CM | Gaucher disease | MGI |
| E75.240 | ICD10CM | Niemann-Pick disease type A | MGI |
| E75.241 | ICD10CM | Niemann-Pick disease type B | MGI |
| E75.242 | ICD10CM | Niemann-Pick disease type C | MGI |
| E75.243 | ICD10CM | Niemann-Pick disease type D | MGI |
| E75.248 | ICD10CM | Other Niemann-Pick disease | MGI |
| E75.249 | ICD10CM | Niemann-Pick disease, unspecified | MGI |
| E75.3 | ICD10CM | Sphingolipidosis, unspecified | MGI |
| E75.6 | ICD10CM | Lipid storage disorder, unspecified | MGI |
| E76 | ICD10CM | Disorders of glycosaminoglycan metabolism | MGI |
| E76.0 | ICD10CM | Mucopolysaccharidosis, type I | MGI |
| E76.01 | ICD10CM | Hurler's syndrome | MGI |
| E76.02 | ICD10CM | Hurler-Scheie syndrome | MGI |
| E76.03 | ICD10CM | Scheie's syndrome | MGI |
| E76.1 | ICD10CM | Mucopolysaccharidosis, type II | MGI |
| E76.2 | ICD10CM | Other mucopolysaccharidoses | MGI |
| E76.21 | ICD10CM | Morquio mucopolysaccharidoses | MGI |
| E76.210 | ICD10CM | Morquio A mucopolysaccharidoses | MGI |
| E76.211 | ICD10CM | Morquio B mucopolysaccharidoses | MGI |
| E76.219 | ICD10CM | Morquio mucopolysaccharidoses, unspecified | MGI |
| E76.22 | ICD10CM | Sanfilippo mucopolysaccharidoses | MGI |
| E76.29 | ICD10CM | Other mucopolysaccharidoses | MGI |
| E76.3 | ICD10CM | Mucopolysaccharidosis, unspecified | MGI |
| E76.8 | ICD10CM | Other disorders of glucosaminoglycan metabolism | MGI |
| E76.9 | ICD10CM | Glucosaminoglycan metabolism disorder, unspecified | MGI |
| E77 | ICD10CM | Disorders of glycoprotein metabolism | MGI |
| E77.0 | ICD10CM | Defects in post-translational modification of lysosomal enzymes | MGI |
| E77.1 | ICD10CM | Defects in glycoprotein degradation | MGI |
| E77.8 | ICD10CM | Other disorders of glycoprotein metabolism | MGI |
| E77.9 | ICD10CM | Disorder of glycoprotein metabolism, unspecified | MGI |
| E78.6 | ICD10CM | Lipoprotein deficiency | MGI |
| E79 | ICD10CM | Disorders of purine and pyrimidine metabolism | MGI |
| E79.0 | ICD10CM | Hyperuricemia without signs of inflammatory arthritis and tophaceous disease | MGI |
| E79.1 | ICD10CM | Lesch-Nyhan syndrome | MGI |
| E79.2 | ICD10CM | Myoadenylate deaminase deficiency | MGI |
| E79.8 | ICD10CM | Other disorders of purine and pyrimidine metabolism | MGI |
| E79.9 | ICD10CM | Disorder of purine and pyrimidine metabolism, unspecified | MGI |
| E80.0 | ICD10CM | Hereditary erythropoietic porphyria | MGI |
| E80.1 | ICD10CM | Porphyria cutanea tarda | MGI |
| E80.2 | ICD10CM | Other and unspecified porphyria | MGI |
| E80.20 | ICD10CM | Unspecified porphyria | MGI |
| E80.21 | ICD10CM | Acute intermittent (hepatic) porphyria | MGI |
| E80.29 | ICD10CM | Other porphyria | MGI |
| E80.3 | ICD10CM | Defects of catalase and peroxidase | MGI |
| E88.1 | ICD10CM | Lipodystrophy, not elsewhere classified | MGI |
| E88.3 | ICD10CM | Tumor lysis syndrome | MGI |
| E88.4 | ICD10CM | Mitochondrial metabolism disorders | MGI |
| E88.40 | ICD10CM | Mitochondrial metabolism disorder, unspecified | MGI |
| E88.41 | ICD10CM | MELAS syndrome | MGI |
| E88.42 | ICD10CM | MERRF syndrome | MGI |
| E88.49 | ICD10CM | Other mitochondrial metabolism disorders | MGI |
| E88.8 | ICD10CM | Other specified metabolic disorders | MGI |
| E88.81 | ICD10CM | Metabolic syndrome | MGI |
| E88.89 | ICD10CM | Other specified metabolic disorders | MGI |
| E88.9 | ICD10CM | Metabolic disorder, unspecified | MGI |
| H49.81 | ICD10CM | Kearns-Sayre syndrome | MGI |
| H49.811 | ICD10CM | Kearns-Sayre syndrome, right eye | MGI |
| H49.812 | ICD10CM | Kearns-Sayre syndrome, left eye | MGI |
| H49.813 | ICD10CM | Kearns-Sayre syndrome, bilateral | MGI |
| H49.819 | ICD10CM | Kearns-Sayre syndrome, unspecified eye | MGI |
| R63.8 | ICD10CM | Other symptoms and signs concerning food and fluid intake | MGI |
| 272.5 | ICD9CM | Lipoprotein deficiencies | MGI |
| 272.6 | ICD9CM | Lipodystrophy | MGI |
| 272.7 | ICD9CM | Lipidoses | MGI |
| 277.1 | ICD9CM | Disorders of porphyrin metabolism | MGI |
| 277.2 | ICD9CM | Other disorders of purine and pyrimidine metabolism | MGI |
| 277.81 | ICD9CM | Primary carnitine deficiency | MGI |
| 277.82 | ICD9CM | Carnitine deficiency due to inborn errors of metabolism | MGI |
| 277.83 | ICD9CM | Iatrogenic carnitine deficiency | MGI |
| 277.84 | ICD9CM | Other secondary carnitine deficiency | MGI |
| 277.85 | ICD9CM | Disorders of fatty acid oxidation | MGI |
| 277.86 | ICD9CM | Peroxisomal disorders | MGI |
| 277.87 | ICD9CM | Disorders of mitochondrial metabolism | MGI |
| 277.88 | ICD9CM | Tumor lysis syndrome | MGI |
| 277.89 | ICD9CM | Other specified disorders of metabolism | MGI |
| 277.9 | ICD9CM | Unspecified disorder of metabolism | MGI |
| 783.9 | ICD9CM | Other symptoms concerning nutrition, metabolism, and development | MGI |
| 794.7 | ICD9CM | Nonspecific abnormal results of function study of basal metabolism | MGI |
| D76.0 | ICD10 | D76.0 Langerhans' cell histiocytosis, not elsewhere classified | UKB |
| E43 | ICD10 | E43 Unspecified severe protein-energy malnutrition | UKB |
| E75.3 | ICD10 | E75.3 Sphingolipidosis, unspecified | UKB |
| E75.6 | ICD10 | E75.6 Lipid storage disorder, unspecified | UKB |
| E77.8 | ICD10 | E77.8 Other disorders of glycoprotein metabolism | UKB |
| E78.6 | ICD10 | E78.6 Lipoprotein deficiency | UKB |
| E79.1 | ICD10 | E79.1 Lesch-Nyhan syndrome | UKB |
| E79.8 | ICD10 | E79.8 Other disorders of purine and pyrimidine metabolism | UKB |
| E80.0 | ICD10 | E80.0 Hereditary erythropoietic porphyria | UKB |
| E80.1 | ICD10 | E80.1 Porphyria cutanea tarda | UKB |
| E80.2 | ICD10 | E80.2 Other porphyria | UKB |
| E88.0 | ICD10 | E88.0 Disorders of plasma-protein metabolism, not elsewhere classified | UKB |
| E88.1 | ICD10 | E88.1 Lipodystrophy, not elsewhere classified | UKB |
| E88.8 | ICD10 | E88.8 Other specified metabolic disorders | UKB |
| E88.9 | ICD10 | E88.9 Metabolic disorder, unspecified | UKB |
| E89.8 | ICD10 | E89.8 Other postprocedural endocrine and metabolic disorders | UKB |
| E89.9 | ICD10 | E89.9 Postprocedural endocrine and metabolic disorder, unspecified | UKB |
| R63.8 | ICD10 | R63.8 Other symptoms and signs concerning food and fluid intake | UKB |
| Z86.2 | ICD10 | Z86.2 Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | UKB |
| 277 | ICD9 | 277 Other and unspecified disorders of metabolism | UKB |
| 277.8 | ICD9 | 2778 Other specified disorders of metabolism | UKB |
| 277.85 | ICD9 | 27785 Other specified disorders of metabolism (histiocytosis x, unspecified) | UKB |
| 277.86 | ICD9 | 27786 Other specified disorders of metabolism (histiocytosis, unspecified) | UKB |
| 277.87 | ICD9 | 27787 Other specified disorders of metabolism (hand-schuller-christian syndrome) | UKB |
| 277.9 | ICD9 | 2779 Unspecified disorders of metabolism | UKB |
| 783.9 | ICD9 | 7839 Other symptoms concerning nutrition, metabolism and development | UKB |
| 794.7 | ICD9 | 7947 Nonspecific abnormal results of basal metabolism function study | UKB |
| V12.2 | ICD9 | V122 Personal history of endocrine, metabolic and immunity disorders | 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.