Preferred Name |
Hereditary coproporphyria |
|
Synonyms |
Porphyria hepatica II |
|
ID |
http://purl.bioontology.org/ontology/SNMI/D6-88320 |
|
altLabel |
Porphyria hepatica II Watson syndrome CPO deficiency Berger-Goldberg syndrome CPRO deficiency |
|
Associated with | ||
cui |
C0162531 C0553586 |
|
notation |
D6-88320 |
|
prefLabel |
Hereditary coproporphyria |
|
SIC |
277.1 |
|
SMX |
(M-27000) (F-66BC0) |
|
tui |
T047 |
|
subClassOf |
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