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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: Angelman Syndrome (D017204)
..Starting node ..Happy puppet syndrome (formerly) (C531619)
Child Nodes:
Sister Nodes:
..Happy puppet syndrome (formerly) (C531619)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4897
Name:	Happy puppet syndrome (formerly)
Definition:
Alternative IDs:
ParentIDs:	MESH:D017204
TreeNumbers:	C10.228.662.075/C531619 \|C16.131.077.095/C531619 \|C16.131.260.040/C531619 \|C16.320.180.040/C531619
Synonyms:
Slim Mappings:	Congenital abnormality\|Genetic disease (inborn)\|Nervous system disease
Reference:	MedGen: C531619 MeSH: C531619 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants