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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: Breast Diseases (D001941)
Parent Node: Lymphocytosis (D008218)
Parent Node: Sclerosis (D012598)
..Starting node ..Sclerosing lymphocytic lobulitis (C537524)
Child Nodes:
Sister Nodes:
..Mediastinal Fibrosis (C536136)
..Mesangial sclerosis, diffuse (C537346)
..Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities (C565405)
..Osteosclerosis with ichthyosis and premature ovarian failure (C536064)
..Poikiloderma, Hereditary Sclerosing (C562824)
..Scleroatonic muscular dystrophy (C537521)
..Sclerosing bone dysplasia mental retardation (C537523)
..Sclerosing lymphocytic lobulitis (C537524)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10065
Name:	Sclerosing lymphocytic lobulitis
Definition:
Alternative IDs:
ParentIDs:	MESH:D001941\|MESH:D008218\|MESH:D012598
TreeNumbers:	C15.378.553.475.604/C537524 \|C17.800.090/C537524 \|C23.550.823/C537524
Synonyms:	Sclerosing lymphocytic lobulitis of the breast
Slim Mappings:	Blood disease\|Pathology (process)\|Skin disease
Reference:	MedGen: C537524 MeSH: C537524 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants