Details of Disease

General Information of Disease (ID: DISU2DYU)

Disease Name Thyroid Hurthle cell carcinoma
Synonyms
oncocytic carcinoma of the thyroid; Hurthle cell thyroid cancer; thyroid cancer, Hurthle cell; follicular thyroid cancer, Hurthle cell type; thyroid carcinoma, Hurthle cell; Hurthle cell thyroid neoplasia; thyroid cancer, follicular, Hurthle cell type
Disease Hierarchy
DISYKSRF: Genetic disease
DISFK2QT: Thyroid gland follicular carcinoma
DISU2DYU: Thyroid Hurthle cell carcinoma
Disease Identifiers
MONDO ID
MONDO_0011836
MESH ID
C536913
UMLS CUI
C0749424
OMIM ID
607464
MedGen ID
196672
SNOMED CT ID
423158009

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
NDUFA13 TTRU1NG Limited Unknown [1]
NDUFA13 TTRU1NG Limited Biomarker [2]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
NDUFA13 OT0UOKIT Limited Unknown [1]
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References

1 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.
2 Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability. Hum Mol Genet. 2015 Jul 15;24(14):3948-55. doi: 10.1093/hmg/ddv133. Epub 2015 Apr 21.