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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: Calcinosis (D002114)
Parent Node: Cardiomyopathies (D009202)
Parent Node: Fetal Death (D005313)
..Starting node ..Cardiomyopathy, fatal fetal, due to myocardial calcification (C543241)
Child Nodes:
Sister Nodes:
..Cardiomyopathy, fatal fetal, due to myocardial calcification (C543241)
..Fetal Resorption (D005327)
..Stillbirth (D050497)
..Thymic Aplasia with Fetal Death (C564768)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1757
Name:	Cardiomyopathy, fatal fetal, due to myocardial calcification
Definition:
Alternative IDs:
ParentIDs:	MESH:D002114\|MESH:D005313\|MESH:D009202
TreeNumbers:	C13.703.223/C543241 \|C14.280.238/C543241 \|C18.452.174.130/C543241 \|C23.550.260.585/C543241
Synonyms:	Myocardial calcifications resulting in intrauterine fetal death
Slim Mappings:	Cardiovascular disease\|Metabolic disease\|Pathology (process)\|Pregnancy complication
Reference:	MedGen: C543241 MeSH: C543241 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants