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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: Fetal Death (D005313)
..Starting node ..Fetal Resorption (D005327)
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:	4257
Name:	Fetal Resorption
Definition:	The disintegration and assimilation of the dead FETUS in the UTERUS at any stage after the completion of organogenesis which, in humans, is after the 9th week of GESTATION. It does not include embryo resorption (see EMBRYO LOSS).
Alternative IDs:
ParentIDs:	MESH:D005313
TreeNumbers:	C13.703.223.300 \|C23.550.260.585.260
Synonyms:	Fetal Resorptions \|Resorption, Fetal \|Resorptions, Fetal
Slim Mappings:	Pathology (process)\|Pregnancy complication
Reference:	MedGen: D005327 MeSH: D005327 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants