GOITER, MULTINODULAR 2
General Information (adopted from Orphanet):
| Synonyms, Signs: |
MNG2 |
| Number of Symptoms | 4 |
| OrphanetNr: | |
| OMIM Id: |
300273
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| ICD-10: |
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| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
X-linked dominant inheritance [Omim] |
| Age of onset: |
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Disease classification (adopted from Orphanet):
| Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0000866) | Euthyroid multinodular goiter | 2 / 7739 | ||||
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(OMIM) | Thyroid volume 22-66ml (adults) | 1 / 7739 | ||||
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(HPO:0001423) | X-linked dominant inheritance | 69 / 7739 | ||||
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(OMIM) | Thyroid goiter (diffuse or nodular) | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
| Description: (OMIM) |
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 ... |