Thyroid hormone metabolism, abnormal, 2

Preferred Label : Thyroid hormone metabolism, abnormal, 2;

Symbol : THMA2;

Type : Phenotype, molecular basis known;

Prefixed ID : #619855;

Details

Origin ID

619855;

UMLS CUI

C5676976;

Genes related to phenotype
- Deiodinase, Iodothyronine, type I [OMIM gene]
ORDO concept(s)
- Short stature-delayed bone age due to thyroid hormone metabolism deficiency [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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