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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: Thyroid Dysgenesis (D050033)
..Starting node ..Lingual Thyroid (D046151)
Child Nodes:
........Lingual Goiter (D047268)
Sister Nodes:
..Hypothyroidism, Congenital, Nongoitrous, 2 (C566852)
..Lingual Thyroid (D046151) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6453
Name:	Lingual Thyroid
Definition:	A condition characterized by the presence of rudimentary THYROID tissue at the base of the TONGUE. It is due to failed embryonic development and migration of thyroid tissue to its normal location. The lingual thyroid usually cannot maintain adequate hormone production thereby resulting in HYPOTHYROIDISM.
Alternative IDs:
ParentIDs:	MESH:D050033
TreeNumbers:	C16.131.894.500 \|C19.874.689.500
Synonyms:	Lingual Thyroids \|Thyroid, Lingual \|Thyroids, Lingual
Slim Mappings:	Congenital abnormality\|Endocrine system disease
Reference:	MedGen: D046151 MeSH: D046151 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants