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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: Hemimegalencephaly (D065705)
Parent Node: Nevus, Sebaceous of Jadassohn (D054000)
..Starting node ..Sebaceous Nevus Syndrome and Hemimegalencephaly (C563339)
Child Nodes:
Sister Nodes:
..Sebaceous Nevus Syndrome and Hemimegalencephaly (C563339)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10090
Name:	Sebaceous Nevus Syndrome and Hemimegalencephaly
Definition:
Alternative IDs:
ParentIDs:	MESH:D054000\|MESH:D065705
TreeNumbers:	C04.557.665.560.700/C563339 \|C05.660.207.536.500/C563339 \|C10.500.507.400.249.500/C563339 \|C10.562.700/C563339 \|C16.131.077.633/C563339 \|C16.131.621.207.532.500/C563339 \|C16.131.666.507.400.249.500/C563339
Synonyms:
Slim Mappings:	Cancer\|Congenital abnormality\|Musculoskeletal disease\|Nervous system disease
Reference:	MedGen: C563339 MeSH: C563339 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants