Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Carcinoma, Papillary (D002291)
Parent Node: Carcinoma, Renal Cell (D002292)
Parent Node: Thyroid Neoplasms (D013964)
..Starting node ..Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia (C565310)
Child Nodes:
Sister Nodes:
..Familial medullary thyroid carcinoma (C536911)
..Nonmedullary thyroid carcinoma, with or without cell oxyphilia (C537842)
..Papillary Thyroid Microcarcinoma (C563277)
..Ruzicka Goerz Anton syndrome (C537192)
..Thyroid cancer, Hurthle cell (C536913)
..Thyroid cancer, medullary (C536914)
..Thyroid cancer, papillary (C536915)
..Thyroid Carcinoma, Nonmedullary 1 (C565247)
..Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia (C565310)
..Thyroid Nodule (D016606)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11052
Name:	Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia
Definition:
Alternative IDs:	OMIM:605642
ParentIDs:	MESH:D002291\|MESH:D002292\|MESH:D013964
TreeNumbers:	C04.557.470.200.025.390/C565310 \|C04.557.470.200.360/C565310 \|C04.557.470.700.360/C565310 \|C04.588.322.894/C565310 \|C04.588.443.915/C565310 \|C04.588.945.947.535.160/C565310 \|C12.758.820.750.160/C565310 \|C12.777.419.473.160/C565310 \|C13.351.937.820.535.160/C56531
Synonyms:	PRN1 \|PTCPRN
Slim Mappings:	Cancer\|Endocrine system disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C565310 MeSH: C565310 OMIM: 605642; Genes:
Phenotypes
Disease Causing ClinVar Variants