Disease browser and phenotype portal

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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: Central Nervous System Neoplasms (D016543)
..Starting node ..Meningeal Neoplasms (D008577)
Child Nodes:
........Meningeal Carcinomatosis (D055756)
........Meningioma (D008579) 3
Sister Nodes:
..Brain Neoplasms (D001932) 30
..Central Nervous System Cysts (D020863) 11
..Meningeal Neoplasms (D008577) 5
..Spinal Cord Neoplasms (D013120) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6941
Name:	Meningeal Neoplasms
Definition:	Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord.
Alternative IDs:
ParentIDs:	MESH:D016543
TreeNumbers:	C04.588.614.250.580 \|C10.551.240.500
Synonyms:	Benign Meningeal Neoplasm \|Benign Meningeal Neoplasms \|Cancer, Meningeal \|Cancers, Meningeal \|Intracranial Meningeal Neoplasm \|Intracranial Meningeal Neoplasms \|Leptomeningeal Neoplasm \|Leptomeningeal Neoplasms \|Malignant Meningeal Neoplasm \|Malignant Meningeal N
Slim Mappings:	Cancer\|Nervous system disease
Reference:	MedGen: D008577 MeSH: D008577 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants