thyroid hormone metabolism, abnormal

Preferred Label : thyroid hormone metabolism, abnormal;

MeSH note : can be caused by mutation of the SECISBP2 gene;

Origin ID

C566454;

UMLS CUI

C1864761;

Currated CISMeF NLP mapping
- Short stature-delayed bone age due to thyroid hormone metabolism deficiency [ORDO Disease]
- Thyroid hormone metabolism, abnormal, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- thyroid diseases [MeSH Descriptor]
Record concept(s)
- thyroid hormone metabolism, abnormal [MeSH concept]
See also inter- (CISMeF)
- Thyroid hormone metabolism, abnormal [OMIM phenotypic series]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Short stature-delayed bone age due to thyroid hormone metabolism deficiency [ORDO Disease]
- Thyroid hormone metabolism, abnormal, 1 [OMIM Phenotype]