sulfhemoglobinemia, congenital

Preferred Label : sulfhemoglobinemia, congenital;

Origin ID

C566102;

UMLS CUI

C1861437;

Currated CISMeF NLP mapping
- Sulfhemoglobinemia, congenital [OMIM Phenotype]
MeSH term(s) associated for indexing
- sulfhemoglobinemia [MeSH Descriptor]
Record concept(s)
- sulfhemoglobinemia, congenital [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Sulfhemoglobinemia, congenital [OMIM Phenotype]