OMOP Concept 434908
Disorder of porphyrin metabolism
StandardConditionSNOMED29094004Disorder
Maps from
10
Descendants
97
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
10 source codes normalize to Disorder of porphyrin metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142013 | Disorder of porphyrin metabolism | Non-standard |
| CIM10 | E80 | Disorders of porphyrin and bilirubin metabolism | Non-standard |
| ICD10 | E80 | Disorders of porphyrin and bilirubin metabolism | Non-standard |
| ICD10CM | E80 | Disorders of porphyrin and bilirubin metabolism | Non-standard |
| ICD10CN | E80 | Disorders of porphyrin and bilirubin metabolism | Non-standard |
| ICD10GM | E80 | Disorders of porphyrin and bilirubin metabolism | Non-standard |
| ICD9CM | 277.1 | Disorders of porphyrin metabolism | Non-standard |
| KCD7 | E80 | Disorders of porphyrin and bilirubin meta- bolism | Non-standard |
| Nebraska Lexicon | 29094004 | Disorder of porphyrin and heme metabolism | Non-standard |
| Read | C371.00 | Disorders of porphyrin metabolism | Non-standard |
Synonyms
Alternative names recorded for Disorder of porphyrin metabolism across source vocabularies.
- Disorder of porphyrin and haem metabolism
- Disorder of porphyrin and heme metabolism
- Disorder of porphyrin metabolism (disorder)
- trastorno del metabolismo de las porfirinas
- trastorno del metabolismo de las porfirinas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(97)Included automatically when you query with descendants.
- 1Disorder of bilirubin metabolism
- 1Ferrochelatase deficiency
- 1Heme oxygenase-1 deficiency
- 1Inherited disorder of porphyrin metabolism
- 1Porphobilinogen deaminase deficiency
- 1Porphyria
- 1Porphyrinopathy
- 1Porphyruria
- 1Uroporphyrinogen decarboxylase deficiency
- 2Acute intermittent porphyria
- 2Bilirubinuria
- 2Chester-type porphyria
- 2Congenital porphyria
- 2Coproporphyria
- 2Delayed conjugation of bilirubin
- 2Disorders of bilirubin excretion
- 2Drug-induced porphyria
- 2Erythropoietic porphyria
- 2Erythropoietic protoporphyria
- 2Exacerbation of porphyria
- 2Hepatic porphyria
- 2Hepatocellular jaundice
- 2Hyperbilirubinemia
- 2Inherited disorder of bilirubin metabolism
- 2Neonatal jaundice with porphyria
- 2Porphyria cutanea tarda
- 2Porphyria-induced phototoxic burn
- 2Progressive intrahepatic cholestasis
- 2Protoporphyrinuria
- 2Secondary porphyria
- 2Uroporphyrinuria
- 2X chromosome-linked sideroblastic anemia
- 3Acquired hyperbilirubinemia
- 3Acquired porphyria cutanea tarda
- 3Arthrogryposis with renal dysfunction and cholestasis syndrome
- 3Congenital erythropoietic porphyria
- 3Conjugated hyperbilirubinemia
- 3Coproporphyrinuria
- 3Crigler-Najjar syndrome
- 3Dubin-Johnson syndrome
- 3Erythropoietic protoporphyria due to ferrochelatase deficiency
- 3Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
- 3Erythropoietic uroporphyria associated with myeloid malignancy
- 3Exacerbation of hepatic porphyria
- 3Exacerbation of hyperbilirubinemia
- 3Familial arthrogryposis-cholestatic hepatorenal syndrome
- 3Familial porphyria cutanea tarda
- 3Gilbert's syndrome
- 3Hereditary coproporphyria
- 3Homozygous acute intermittent porphyria
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