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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: Cerebrovascular Disorders (D002561)
Parent Node: Headache Disorders, Secondary (D051271)
..Starting node ..Vascular Headaches (D014653)
Child Nodes:
Sister Nodes:
..Post-Dural Puncture Headache (D051299)
..Post-Traumatic Headache (D051298)
..Vascular Headaches (D014653)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11529
Name:	Vascular Headaches
Definition:	Secondary headache disorders attributed to a variety of cranial or cervical vascular disorders, such as BRAIN ISCHEMIA; INTRACRANIAL HEMORRHAGES; and CENTRAL NERVOUS SYSTEM VASCULAR MALFORMATIONS.
Alternative IDs:
ParentIDs:	MESH:D002561\|MESH:D051271
TreeNumbers:	C10.228.140.300.800 \|C10.228.140.546.699.500 \|C14.907.253.937
Synonyms:	Cephalgias, Vascular \|Cephalgia, Vascular \|Headaches, Vascular \|Headache, Vascular \|Vascular Cephalgia \|Vascular Cephalgias \|Vascular Headache
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D014653 MeSH: D014653 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants