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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: Chromosome Deletion (D002872)
Parent Node: Prader-Willi Syndrome (D011218)
..Starting node ..Prader-Willi-Like Syndrome Associated With Chromosome 6 (C566764)
Child Nodes:
Sister Nodes:
..Prader-Willi habitus, osteopenia, and camptodactyly (C538276)
..Prader-Willi-Like Syndrome Associated With Chromosome 6 (C566764)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9200
Name:	Prader-Willi-Like Syndrome Associated With Chromosome 6
Definition:
Alternative IDs:
ParentIDs:	MESH:D002872\|MESH:D011218
TreeNumbers:	C10.597.606.643.690/C566764 \|C16.131.077.730/C566764 \|C16.131.260.700/C566764 \|C16.320.180.700/C566764 \|C18.654.726.500.740/C566764 \|C23.550.210.050.500.500/C566764
Synonyms:
Slim Mappings:	Congenital abnormality\|Genetic disease (inborn)\|Nervous system disease\|Nutrition disorder\|Pathology (process)
Reference:	MedGen: C566764 MeSH: C566764 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants