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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 ..Histiocytosis (D015614)
Child Nodes:
........Histiocytic Disorders, Malignant (D015620) 4
........Histiocytosis with joint contractures and sensorineural deafness (C538322)
........Histiocytosis, Familial Lipochrome (C562738)
........Histiocytosis, Langerhans-Cell (D006646) 3
........Histiocytosis, Non-Langerhans-Cell (D015616) 19
........Histiocytosis, Progressive Mucinous (C564186)
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:	5216
Name:	Histiocytosis
Definition:	General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT.
Alternative IDs:
ParentIDs:	MESH:D008206
TreeNumbers:	C15.604.250
Synonyms:	Histiocytoses
Slim Mappings:	Lymphatic disease
Reference:	MedGen: D015614 MeSH: D015614 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants