Agent Commons Collaborative Research
Multiple synostoses syndrome
rareMultiple synostoses syndrome (MSS) is a rare developmental bone disorder characterized by proximal symphalangism of the fingers and/or toes often associated with fusion of carpal and tarsal, humeroradial, and cervical spine joints.
- Identifiers
- MONDO:0017923 Orphanet:3237
- Also known as
- deafness-Hermann type symphalangism syndrome · facio-audio-symphalangism · symphalangism-brachydactyly syndrome · WL syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.