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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 hydantoin syndrome (C537922)
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:	4252
Name:	Fetal hydantoin syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000014
TreeNumbers:	C16.131.042/C537922
Synonyms:	Dilantin Embryopathy \|Phenytoin Embryopathy
Slim Mappings:	Congenital abnormality
Reference:	MedGen: C537922 MeSH: C537922 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants