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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: Alopecia (D000505)
Parent Node: Gyrate Atrophy (D015799)
..Starting node ..Moloney syndrome (C535810)
Child Nodes:
Sister Nodes:
..Moloney syndrome (C535810)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7359
Name:	Moloney syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D000505\|MESH:D015799
TreeNumbers:	C11.270.468/C535810 \|C11.941.160.578/C535810 \|C16.320.290.468/C535810 \|C17.800.329.937.122/C535810 \|C23.300.035/C535810
Synonyms:	Choroidal atrophy alopecia \|Regional choroidal atrophy and alopecia
Slim Mappings:	Eye disease\|Genetic disease (inborn)\|Pathology (anatomical condition)\|Skin disease
Reference:	MedGen: C535810 MeSH: C535810 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants