diabetes mellitus, neonatal, with congenital hypothyroidism

Preferred Label : diabetes mellitus, neonatal, with congenital hypothyroidism;

Origin ID

C565705;

UMLS CUI

C1857775;

Currated CISMeF NLP mapping
- Diabetes mellitus, neonatal, with congenital hypothyroidism [OMIM Phenotype]
- NDH syndrome [Disease (Nov.)]
- Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome [ORDO Disease]
- neonatal diabetes mellitus with congenital hypothyroidism [DO Concept]
MeSH term(s) associated for indexing
- congenital hypothyroidism [MeSH Descriptor]
- diabetes mellitus [MeSH Descriptor]
Record concept(s)
- diabetes mellitus, neonatal, with congenital hypothyroidism [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Diabetes mellitus, neonatal, with congenital hypothyroidism [OMIM Phenotype]
- NDH syndrome [Disease (Nov.)]
- Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome [ORDO Disease]
- neonatal diabetes mellitus with congenital hypothyroidism [DO Concept]