MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: adenocarcinoma (MONDO:0004970)
Parent Node: thyroid gland carcinoma (MONDO:0015075)
..Starting node ..thyroid gland adenocarcinoma ()
Child Nodes:
........thyroid gland follicular carcinoma ()
........thyroid gland mucoepidermoid carcinoma ()
........thyroid gland papillary carcinoma ()
Sister Nodes:
..differentiated thyroid carcinoma ()
..familial nonmedullary thyroid carcinoma ()
..multiple endocrine neoplasia type 2 ()
..thyroid gland adenocarcinoma ()
..thyroid gland spindle cell tumor with thymus-like differentiation ()
..thyroid gland squamous cell carcinoma ()
..thyroid gland undifferentiated (anaplastic) carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	24622
Name:	thyroid gland adenocarcinoma
Definition:	An adenocarcinoma arising from the follicular cells of the thyroid gland. According to the degree of differentiation, it is classified either as differentiated carcinoma (extensive evidence of follicular cell differentiation), or poorly differentiated carcinoma (limited evidence of follicular cell differentiation).
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	thyroid adenocarcinoma; thyroid gland adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
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