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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: Foot Deformities (D005530)
..Starting node ..Hammer Toe Syndrome (D037801)
Child Nodes:
Sister Nodes:
..Flatfoot (D005413)
..Foot Deformities, Acquired (D005531) 4
..Foot Deformities, Congenital (D005532) 78
..Hallux Valgus (D006215)
..Hallux Varus (D050488) 2
..Hammer Toe Syndrome (D037801)
..Kantaputra Gorlin syndrome (C535547)
..Krauss Herman Holmes syndrome (C537618)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4881
Name:	Hammer Toe Syndrome
Definition:	A condition characterized by a series of interrelated digital symptoms and joint changes of the lesser digits and METATARSOPHALANGEAL JOINTS of the FOOT. The syndrome can include some or all of the following conditions: hammer toe, claw toe, mallet toe, overlapping fifth toe, curly toe, EXOSTOSIS; HYPEROSTOSIS; interdigital heloma, or contracted toe.
Alternative IDs:
ParentIDs:	MESH:D005530
TreeNumbers:	C05.330.615
Synonyms:	Clawtoe \|Claw Toe \|Clawtoes \|Claw Toes \|Hammer Toe \|Hammer Toes \|Hammertoe Syndrome \|Hammertoe Syndromes \|Mallet Toe \|Mallet Toes \|Syndrome, Hammertoe \|Syndrome, Hammer Toe \|Syndromes, Hammertoe \|Toe, Claw \|Toe, Hammer \|Toe, Mallet \|Toes, Claw \|Toes, Hammer \|Toes, Mallet
Slim Mappings:	Musculoskeletal disease
Reference:	MedGen: D037801 MeSH: D037801 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants