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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: Angiomatosis (D000798)
Parent Node: Brain Neoplasms (D001932)
..Starting node ..Familial capillaro-venous leptomeningeal angiomatosis (C536609)
Child Nodes:
Sister Nodes:
..Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert (C536367)
..Cerebral astrocytoma, adult (C535354)
..Cerebral sarcoma (C537946)
..Cerebral Ventricle Neoplasms (D002551) 3
..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
..Desmoplastic cerebral astrocytoma of infancy (C535945)
..Familial capillaro-venous leptomeningeal angiomatosis (C536609)
..Glioma of Brain, Familial (C564230)
..Infratentorial Neoplasms (D015192) 2
..Neurocytoma (D018306)
..Pascual Castroviejo syndrome (C536302)
..Pinealoma (D010871) 1
..PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (OMIM:603688)
..Rhabdoid Tumor Predisposition Syndrome 1 (C563738)
..Supratentorial Neoplasms (D015173) 8
..Turcot syndrome (C536928)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4124
Name:	Familial capillaro-venous leptomeningeal angiomatosis
Definition:
Alternative IDs:
ParentIDs:	MESH:D000798\|MESH:D001932
TreeNumbers:	C04.588.614.250.195/C536609 \|C10.228.140.211/C536609 \|C10.551.240.250/C536609 \|C14.907.077/C536609
Synonyms:
Slim Mappings:	Cancer\|Cardiovascular disease\|Nervous system disease
Reference:	MedGen: C536609 MeSH: C536609 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants