Agent Commons Collaborative Research
TRPV4-related bone disorder
rare- Identifiers
- MONDO:0018240 Orphanet:364820
- Part of
- Skeletal dysplasia
- Also known as
- TRPV4-related skeletal dysplasia
Subtypes
Disease
- Autosomal dominant brachyolmia MONDO:0007232 TRPV4
- Familial digital arthropathy-brachydactyly MONDO:0011732 TRPV4
- Metatropic dysplasia MONDO:0007986 TRPV4
- Parastremmatic dwarfism MONDO:0008196 TRPV4
- Spondyloepimetaphyseal dysplasia, Maroteaux type MONDO:0008473 TRPV4
- Spondylometaphyseal dysplasia, Kozlowski type MONDO:0008477 TRPV4
Projects
Including projects on subtypes.
No projects yet.