Goiter, multinodular 2

Preferred Label : Goiter, multinodular 2;

Symbol : MNG2;

CISMeF acronym : MNG2;

Type : Phenotype or locus, molecular basis unknown;

Description : Multinodular goiter is a common disorder characterized by nodular enlargement of the thyroid gland. It occurs with a female:male ratio of 5:1 (summary by Capon et al., 2000). For additional phenotypic information and a discussion of genetic heterogeneity of multinodular goiter, see MNG1 (138800).;

Inheritance : X-linked dominant;

Prefixed ID : %300273;

Details

Origin ID

300273;

UMLS CUI

C1846033;

Currated CISMeF NLP mapping
- goiter, multinodular 2 [MeSH concept]
- goiter, multinodular 2 [MeSH Supplementary Concept]
DO Cross reference
- multinodular goiter [DO Concept]
HPO term(s)
- Euthyroid multinodular goiter [HPO term]
- X-linked dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- goiter, multinodular 2 [MeSH Supplementary Concept]
- goiter, multinodular 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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