Disease browser and phenotype portal

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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 (D001847)
Parent Node: Bone Diseases, Infectious (D001850)
..Starting node ..Osteitis (D010000)
Child Nodes:
Sister Nodes:
..Osteitis (D010000)
..Osteomyelitis (D010019) 7
..Periostitis (D010522) 1
..Spondylitis (D013166) 10
..Tuberculosis, Osteoarticular (D014394) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8367
Name:	Osteitis
Definition:
Alternative IDs:
ParentIDs:	MESH:D001847\|MESH:D001850
TreeNumbers:	C01.539.160.412 \|C05.116.165.412 \|C05.116.680
Synonyms:	Bone Inflammation \|Inflammation, Bone
Slim Mappings:	Bacterial infection or mycosis\|Musculoskeletal disease
Reference:	MedGen: D010000 MeSH: D010000 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants