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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: Bone Diseases, Developmental (D001848)
Parent Node: Genu Varum (D056305)
..Starting node ..Weismann Netter syndrome (C537082)
Child Nodes:
Sister Nodes:
..Weismann Netter syndrome (C537082)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11724
Name:	Weismann Netter syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D001848\|MESH:D056305
TreeNumbers:	C05.116.099/C537082 \|C05.116.511/C537082
Synonyms:	Anterior bowing of legs with dwarfism \|Bowing of legs, anterior, with dwarfism \|Toxopachyosteose diaphysaire tibio-peroniere \|Toxopachyosteosis \|Toxopachyoteose diaphysaire tibio peroniere \|Weismann Netter Stuhl syndrome \|Weismann-Netter Syndrome
Slim Mappings:	Musculoskeletal disease
Reference:	MedGen: C537082 MeSH: C537082 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants