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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: Congenital Abnormalities (D000013)
Parent Node: Lymphatic Diseases (D008206)
..Starting node ..Lymphatic Abnormalities (D044148)
Child Nodes:
........22q11 Deletion Syndrome (D058165) 5
........Lymphangiectasis, Intestinal (D008201) 3
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:	6590
Name:	Lymphatic Abnormalities
Definition:	Congenital or acquired structural abnormalities of the lymphatic system (LYMPHOID TISSUE) including the lymph vessels.
Alternative IDs:
ParentIDs:	MESH:D000013\|MESH:D008206
TreeNumbers:	C15.604.451 \|C16.131.482
Synonyms:	Abnormalities, Lymphatic \|Abnormality, Lymphatic \|Lymphatic Abnormality
Slim Mappings:	Congenital abnormality\|Lymphatic disease
Reference:	MedGen: D044148 MeSH: D044148 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants