hypothyroidism, congenital, nongoitrous, 3

Preferred Label : hypothyroidism, congenital, nongoitrous, 3;

MeSH synonym : congenital hypothyroidism, nongoitrous, 3;

Origin ID

C567935;

UMLS CUI

C2940785;

Automatic exact mappings (from CISMeF team)
- congenital nongoitrous hypothyroidism 3 [DO Concept]
Currated CISMeF NLP mapping
- Hypothyroidism, congenital, nongoitrous, 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- congenital hypothyroidism [MeSH Descriptor]
Record concept(s)
- hypothyroidism, congenital, nongoitrous, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypothyroidism, congenital, nongoitrous, 3 [OMIM Phenotype]