Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism

Preferred Label : Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 206400;

Details

Origin ID

206400;

UMLS CUI

C1859785;

Automatic exact mappings (from CISMeF team)
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH concept]
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH Supplementary Concept]
DO Cross reference
- congenital nonspherocytic hemolytic anemia [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Elevated urinary delta-aminolevulinic acid [HPO term]
- Jaundice [HPO term]
- Nonspherocytic hemolytic anemia [HPO term]
- Splenomegaly [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH Supplementary Concept]
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients