Preferred Name |
hereditary coproporphyria |
|
Synonyms |
Coproporphyrinogen oxidase deficiency |
|
Definitions |
OMIM mapping confirmed by DO. [SN]. |
|
ID |
http://purl.obolibrary.org/obo/DOID_13269 |
|
comment |
OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
OMIM:121300 MESH:D046349 ICD10CM:E80.29 UMLS_CUI:C0162531 SNOMEDCT_US_2023_03_01:7425008 GARD:6619 NCI:C84759 |
|
has exact synonym |
Coproporphyrinogen oxidase deficiency hereditary coproporphyria porphyria |
|
has material basis in | ||
has_obo_namespace |
disease_ontology |
|
id |
DOID:13269 |
|
in_subset | ||
label |
hereditary coproporphyria |
|
notation |
DOID:13269 |
|
prefLabel |
hereditary coproporphyria |
|
subClassOf |
Create mapping