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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: Lymphatic Diseases (D008206)
..Starting node ..Thymus Hyperplasia (D013952)
Child Nodes:
Sister Nodes:
..Capillary Malformation Of The Lower Lip, Lymphatic Malformation Of Face And Neck, Asymmetry Of Face And Limbs, And Partial/Generalized Overgrowth (C567763)
..Histiocytosis (D015614) 32
..Lymphadenitis (D008199) 5
..Lymphangiectasis (D008200) 5
..Lymphangitis (D008205)
..Lymphatic Abnormalities (D044148) 10
..Lymphedema (D008209) 21
..Lymphocele (D008210) 1
..Lymphoproliferative Disorders (D008232) 126
..Mucocutaneous Lymph Node Syndrome (D009080) 1
..Pseudolymphoma (D019310)
..Splenic Diseases (D013158) 17
..Thymus Hyperplasia (D013952)
..Thymus Neoplasms (D013953) 3
..Tuberculosis, Lymph Node (D014388) 1
..Vasculitis, Lymphocytic, Nodular (C566008)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11040
Name:	Thymus Hyperplasia
Definition:	Enlargement of the thymus. A condition described in the late 1940's and 1950's as pathological thymic hypertrophy was status thymolymphaticus and was treated with radiotherapy. Unnecessary removal of the thymus was also practiced. It later became apparent that the thymus undergoes normal physiological hypertrophy, reaching a maximum at puberty and involuting thereafter. The concept of status thymolymphaticus has been abandoned. Thymus hyperplasia is present in two thirds of all patients with myasthenia gravis. (From Segen, Dictionary of Modern Medicine, 1992; Cecil Textbook of Medicine, 19th ed, p1486)
Alternative IDs:
ParentIDs:	MESH:D008206
TreeNumbers:	C15.604.816
Synonyms:	Gland Hyperplasias, Thymus \|Gland Hyperplasia, Thymus \|Hyperplasia of Thymus Gland \|Hyperplasias, Thymic \|Hyperplasia, Thymic \|Hyperplasia, Thymus \|Thymic Hyperplasia \|Thymic Hyperplasias \|Thymus Gland Hyperplasia \|Thymus Gland Hyperplasias
Slim Mappings:	Lymphatic disease
Reference:	MedGen: D013952 MeSH: D013952 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants