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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: Abnormalities, Drug-Induced (D000014)
..Starting node ..Fetal trimethadione syndrome (C537798)
Child Nodes:
Sister Nodes:
..Accutane embryopathy (C535670)
..Acitretin embryopathy (C538169)
..Fetal hydantoin syndrome (C537922)
..Fetal trimethadione syndrome (C537798)
..Ho Kaufman Mcalister syndrome (C538325)
..Isotretinoin embryopathy like syndrome (C535542)
..Valproic acid antenatal infection (C536525)
..Warfarin syndrome (C536683)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4258
Name:	Fetal trimethadione syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000014
TreeNumbers:	C16.131.042/C537798
Synonyms:	Trimethadione embryopathy
Slim Mappings:	Congenital abnormality
Reference:	MedGen: C537798 MeSH: C537798 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants