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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: Angiomatosis (D000798)
Parent Node: Breast Diseases (D001941)
Parent Node: Hyperplasia (D006965)
..Starting node ..Pseudoangiomatous stromal hyperplasia (C535824)
Child Nodes:
Sister Nodes:
..Facial Hemihypertrophy (C563014)
..Hemihyperplasia, Isolated (C565524)
..Pseudoangiomatous stromal hyperplasia (C535824)
..Sebaceous gland hyperplasia, familial presenile (C537530)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9406
Name:	Pseudoangiomatous stromal hyperplasia
Definition:
Alternative IDs:
ParentIDs:	MESH:D000798\|MESH:D001941\|MESH:D006965
TreeNumbers:	C14.907.077/C535824 \|C17.800.090/C535824 \|C23.550.444/C535824
Synonyms:	Mammary pseudoangiomatous stromal hyperplasia \|Pseudoangiomatous stromal hyperplasia of the breast
Slim Mappings:	Cardiovascular disease\|Pathology (process)\|Skin disease
Reference:	MedGen: C535824 MeSH: C535824 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants