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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: Leiomyomatosis (D018231)
Parent Node: Skin Neoplasms (D012878)
Parent Node: Uterine Neoplasms (D014594)
..Starting node ..Reed's syndrome (C535516)
Child Nodes:
Sister Nodes:
..Adenosarcoma of the uterus (C538232)
..Endometrial Neoplasms (D016889) 3
..Leiomyoma of vulva and esophagus (C537006)
..Reed's syndrome (C535516)
..Uterine Cervical Neoplasms (D002583) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9627
Name:	Reed's syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D012878\|MESH:D014594\|MESH:D018231
TreeNumbers:	C04.557.450.590.450.465/C535516 \|C04.588.805/C535516 \|C04.588.945.418.948/C535516 \|C13.351.500.852.762/C535516 \|C13.351.937.418.875/C535516 \|C17.800.882/C535516
Synonyms:	Cutaneous leiomyomata with uterine leiomyomata \|Hereditary leiomyomatosis and renal cell cancer \|Leiomyoma, hereditary multiple, of skin \|Leiomyoma, multiple cutaneous \|Leiomyomatosis and renal cell cancer, hereditary \|Multiple cutaneous and uterine leiomyoma
Slim Mappings:	Cancer\|Skin disease\|Urogenital disease (female)
Reference:	MedGen: C535516 MeSH: C535516 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants