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1279836009: Familial multinodular goiter syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5234049010 A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234050010 A rare thyroid disease characterised by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234042018 Familial multinodular goiter syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5234043011 Familial multinodular goiter syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5234044017 FMNG - familial multinodular goitre en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234045016 Familial multinodular goiter en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5234046015 Familial multinodular goitre en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5234047012 FMNG - familial multinodular goiter en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234048019 Familial multinodular goitre syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Is a Familial disease true Inferred relationship Some
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Is a Multinodular goiter true Inferred relationship Some
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Finding site Entire thyroid gland true Inferred relationship Some 1
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Finding site Thyroid structure true Inferred relationship Some 2
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Associated morphology Multinodular hyperplasia true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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