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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: Hearing Loss, Sensorineural (D006319)
Parent Node: Paraganglioma (D010235)
..Starting node ..Paragangliomas with Sensorineural Hearing Loss (C566831)
Child Nodes:
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:	8594
Name:	Paragangliomas with Sensorineural Hearing Loss
Definition:
Alternative IDs:
ParentIDs:	MESH:D006319\|MESH:D010235
TreeNumbers:	C04.557.465.625.650.700/C566831 \|C04.557.580.625.650.700/C566831 \|C09.218.458.341.887/C566831 \|C10.597.751.418.341.887/C566831 \|C23.888.592.763.393.341.887/C566831
Synonyms:
Slim Mappings:	Cancer\|Ear-nose-throat disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: C566831 MeSH: C566831 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants