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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: Osteochondritis (D010007)
..Starting node ..Freiberg's disease (C535636)
Child Nodes:
Sister Nodes:
..Freiberg's disease (C535636)
..Nathalie syndrome (C538342)
..Osteochondritis Dissecans (D010008) 2
..Ruvalcaba Syndrome (C579395)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4414
Name:	Freiberg's disease
Definition:
Alternative IDs:
ParentIDs:	MESH:D010007
TreeNumbers:	C05.116.791/C535636 \|C05.182.520/C535636 \|C17.300.182.520/C535636
Synonyms:	Freiberg-Kohler syndrome \|Freiberg's infraction \|Kohler's second disease \|Second metatarsal osteochondrosis
Slim Mappings:	Connective tissue disease\|Musculoskeletal disease
Reference:	MedGen: C535636 MeSH: C535636 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants