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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: Arteriovenous Malformations (D001165)
Parent Node: Hemangioma (D006391)
..Starting node ..Spinal Arterial Venous Malformations with Cutaneous Hemangiomas (C566282)
Child Nodes:
Sister Nodes:
..Angioma hereditary neurocutaneous (C536364)
..Central Nervous System Venous Angioma (D020787)
..Hemangioendothelioma (D006390) 3
..Hemangioma, Capillary (D018324) 3
..Hemangioma, Cavernous (D006392) 3
..Hemangiomas of Small Intestine (C564201)
..Hemangiomatosis, Cutaneous, with Associated Features (C562438)
..Hemangiomatosis, Disseminated (C566283)
..Kasabach-Merritt Syndrome (D059885) 1
..Littoral cell angioma of the spleen (C537031)
..Pascual Castroviejo syndrome (C536302)
..Spinal Arterial Venous Malformations with Cutaneous Hemangiomas (C566282)
..Sturge-Weber Syndrome (D013341) 1
..Tufted angioma (C536924)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10456
Name:	Spinal Arterial Venous Malformations with Cutaneous Hemangiomas
Definition:
Alternative IDs:
ParentIDs:	MESH:D001165\|MESH:D006391
TreeNumbers:	C04.557.645.375/C566282 \|C14.240.850.750/C566282 \|C14.907.150/C566282 \|C16.131.240.850.750/C566282
Synonyms:
Slim Mappings:	Cancer\|Cardiovascular disease\|Congenital abnormality
Reference:	MedGen: C566282 MeSH: C566282 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants