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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: Osteochondrodysplasias (D010009)
Parent Node: Osteolysis (D010014)
..Starting node ..Osebold Skeletal Dysplasia Osteolysis Syndrome (C566380)
Child Nodes:
Sister Nodes:
..Acro-Osteolysis (D030981) 7
..Dermatoosteolysis Kirghizian type (C535373)
..Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome (C564357)
..Osebold Skeletal Dysplasia Osteolysis Syndrome (C566380)
..Osteolysis hereditary multicentric (C536051)
..Osteolysis syndrome recessive (C536052)
..Osteolysis, Essential (D010015) 1
..Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy (C567171)
..Polyosteolysis-Hyperostosis Syndrome (C563658)
..Polyostotic osteolytic dysplasia, hereditary expansile (C536335)
..Talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals (C536894)
..Winchester syndrome (C536709)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8357
Name:	Osebold Skeletal Dysplasia Osteolysis Syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D010009\|MESH:D010014
TreeNumbers:	C05.116.099.708/C566380 \|C05.116.264.579/C566380
Synonyms:
Slim Mappings:	Musculoskeletal disease
Reference:	MedGen: C566380 MeSH: C566380 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants