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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: Scleroderma, Localized (D012594)
Parent Node: Scleroderma, Systemic (D012595)
..Starting node ..Juvenile-onset scleroderma (C543759)
Child Nodes:
Sister Nodes:
..Juvenile systemic scleroderma (C537703)
..Juvenile-onset scleroderma (C543759)
..REYNOLDS SYNDROME (OMIM:613471)
..Scleroderma, Diffuse (D045743)
..SCLERODERMA, FAMILIAL PROGRESSIVE (OMIM:181750)
..Scleroderma, Limited (D045745) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5998
Name:	Juvenile-onset scleroderma
Definition:
Alternative IDs:
ParentIDs:	MESH:D012594\|MESH:D012595
TreeNumbers:	C17.300.787/C543759 \|C17.300.799/C543759 \|C17.800.767/C543759 \|C17.800.784/C543759
Synonyms:	Juvenile Scleroderma
Slim Mappings:	Connective tissue disease\|Skin disease
Reference:	MedGen: C543759 MeSH: C543759 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants