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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: Neoplasms (D009369)
..Starting node ..Paraneoplastic Syndromes (D010257)
Child Nodes:
........Humoral Hypercalcemia Of Malignancy (C562390)
........Paraneoplastic Endocrine Syndromes (D009384) 2
........Paraneoplastic Syndromes, Nervous System (D020361) 10
........Paraneoplastic Syndromes, Ocular (D059545)
Sister Nodes:
..abc disease (C579754)
..Chromosomal Instability with Tissue-Specific Radiosensitivity (C565848)
..Cysts (D003560) 78
..Hamartoma (D006222) 26
..Neoplasms by Histologic Type (D009370) 696
..Neoplasms by Site (D009371) 492
..Neoplasms, Experimental (D009374) 37
..Neoplasms, Hormone-Dependent (D009376)
..Neoplasms, Multiple Primary (D009378) 24
..Neoplasms, Post-Traumatic (D017169)
..Neoplasms, Radiation-Induced (D009381) 3
..Neoplasms, Second Primary (D016609)
..Neoplastic Processes (D009385) 18
..Neoplastic Syndromes, Hereditary (D009386) 111
..Paraneoplastic Syndromes (D010257) 16
..Precancerous Conditions (D011230) 29
..Pregnancy Complications, Neoplastic (D011252) 7
..Tumor Virus Infections (D014412) 20
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8611
Name:	Paraneoplastic Syndromes
Definition:	In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products.
Alternative IDs:
ParentIDs:	MESH:D009369
TreeNumbers:	C04.730
Synonyms:	Paraneoplastic Syndrome \|Syndrome, Paraneoplastic \|Syndromes, Paraneoplastic
Slim Mappings:	Cancer
Reference:	MedGen: D010257 MeSH: D010257 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants