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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

Disease Browser
Parent Node: Goiter (D006042)
..Starting node ..Goiter, Nodular (D006044)
Child Nodes:
........Arrhenoblastoma--Thyroid Adenoma (C566256)
........Daneman Davy Mancer syndrome (C535986)
........Euthyroid Goiter (C562732) 1
........Goiter, Multinodular 2 (C564546)
........Goiter, Multinodular 3 (C565260)
........Pendred syndrome (C536648)
........Thyroid Adenoma, Hyperfunctioning (C566386)
Sister Nodes:
..Bangstad syndrome (C537902)
..Goiter, Endemic (D006043)
..Goiter, Nodular (D006044) 8
..Goiter, Substernal (D006045)
..Graves Disease (D006111) 3
..Lingual Goiter (D047268)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4749
Name:	Goiter, Nodular
Definition:	An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS.
Alternative IDs:
ParentIDs:	MESH:D006042
TreeNumbers:	C19.874.283.501
Synonyms:	Goiters, Nodular \|Nodular Goiter \|Nodular Goiters
Slim Mappings:	Endocrine system disease
Reference:	MedGen: D006044 MeSH: D006044 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants