Flatfoot
Disease ID: disease_node_3269
Connections displayed (default: 10).
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| Dbxref | GARD:5488, MEDDRA:10066242, MESH:D005413, MIM:192950, ORDO:178382, SNOMEDCT_US_2023_03_01:205359003, UMLS_CUI:C0240912 |
|---|---|
| Subclassof | DOID_0050736, DOID_0080015, DOID_65 |
| Data Source | DOID, MESH |
| Synonyms | CVT, congenital convex foot, congenital convex pes valgus, congenital rocker-bottom foot, rocker-bottom foot deformity |
| Mesh Id | D005413 |
| Mesh Label | Flatfoot |
| Mesh Subclassof | D000070558 |
| Doid Label | congenital vertical talus |
| Doid Description | A connective tissue disease characterized by dislocation of the talonavicular joint with vertical orientation of the talus and rigid dorsal dislocation of the navicular, equinus deformity of the calcaneus, abduction deformity of the forefoot, and contracture of the soft tissues of the hind- and mid-foot that has_material_basis_in heterozygous mutation in the HOXD10 gene on chromosome 2q31.1. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_3269 |
| Doid Id | DOID_0111568 |
| Disease Has Basis In | HP_0001197 |
| Label | Flatfoot |
- Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Connective Tissue Diseases(ID:disease_node_2242) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)