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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: Paraganglioma (D010235)
..Starting node ..Paraganglioma, Extra-Adrenal (D010236)
Child Nodes:
........Abdominal chemodectomas with cutaneous angiolipomas (C535552)
........Carney Triad (C565803)
........Carotid Body Tumor (D002345)
........Glomus Jugulare Tumor (D005925)
........Glomus Tympanicum Tumor (D043604)
........Glomus vagale tumors (C536827)
Sister Nodes:
..Carney-Stratakis Syndrome (C564650)
..Paraganglioma, Extra-Adrenal (D010236) 6
..Paragangliomas 2 (C566646)
..Paragangliomas 3 (C565335)
..PARAGANGLIOMAS 4 (OMIM:115310)
..Paragangliomas with Sensorineural Hearing Loss (C566831)
..Pheochromocytoma (D010673) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8590
Name:	Paraganglioma, Extra-Adrenal
Definition:	A relatively rare, usually benign neoplasm originating in the chemoreceptor tissue of the CAROTID BODY; GLOMUS JUGULARE; GLOMUS TYMPANICUM; AORTIC BODIES; and the female genital tract. It consists histologically of rounded or ovoid hyperchromatic cells that tend to be grouped in an alveolus-like pattern within a scant to moderate amount of fibrous stroma and a few large thin-walled vascular channels. (From Stedman, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D010235
TreeNumbers:	C04.557.465.625.650.700.705 \|C04.557.580.625.650.700.705
Synonyms:	Chemodectoma \|Chemodectomas \|Extra-Adrenal Paraganglioma \|Extra-Adrenal Paragangliomas \|Nonchromaffin Paraganglioma \|Non-Chromaffin Paraganglioma \|Nonchromaffin Paragangliomas \|Non-Chromaffin Paragangliomas \|Paraganglioma, Extra Adrenal \|Paraganglioma, Nonchromaf
Slim Mappings:	Cancer
Reference:	MedGen: D010236 MeSH: D010236 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants