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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: Pathological Conditions, Anatomical (D020763)
Parent Node: Precancerous Conditions (D011230)
..Starting node ..Leukoplakia (D007971)
Child Nodes:
........Leukoplakia, Oral (D007972) 1
Sister Nodes:
..Aberrant Crypt Foci (D058739)
..Erythroplasia (D004919)
..Keratosis, Actinic (D055623) 1
..Leukoplakia (D007971) 2
..Lymphomatoid Granulomatosis (D008230)
..Preleukemia (D011289)
..Uterine Cervical Dysplasia (D002578) 2
..Xeroderma Pigmentosum (D014983) 16
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6404
Name:	Leukoplakia
Definition:	A white patch lesion found on a MUCOUS MEMBRANE that cannot be scraped off. Leukoplakia is generally considered a precancerous condition, however its appearance may also result from a variety of HEREDITARY DISEASES.
Alternative IDs:
ParentIDs:	MESH:D011230\|MESH:D020763
TreeNumbers:	C04.834.512 \|C23.300.816
Synonyms:	Lesion, Leukoplakic \|Lesions, Leukoplakic \|Leukokeratoses \|Leukokeratosis \|Leukoplakias \|Leukoplakic Lesion \|Leukoplakic Lesions
Slim Mappings:	Cancer\|Pathology (anatomical condition)
Reference:	MedGen: D007971 MeSH: D007971 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants