Acetophenetidin sensitivity

Preferred Label : Acetophenetidin sensitivity;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 200300;

Details

Origin ID

200300;

UMLS CUI

C1860214;

HPO term(s)
- Abnormality of blood and blood-forming tissues [HPO term]
- Autosomal recessive inheritance [HPO term]
- Hemolytic anemia [HPO term]
- Methemoglobinemia [HPO term]
See also inter- (CISMeF)
- poisoning by phenacetin [SNOMED Notion]
Semantic type(s)
- Finding [UMLS semantic type]

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