VWDE
Description
The VWDE (von Willebrand factor D and EGF domains) is a protein-coding gene located on chromosome 7.
VWDE is also known as -.
Associated Diseases
- type 1 diabetes mellitus
- secondary polycythemia
- hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
- dentin dysplasia type I
- tooth agenesis, selective, 7
- amelogenesis imperfecta type 3B
- amelogenesis imperfecta hypomaturation type 2A4
- dentin dysplasia type II
- amelogenesis imperfecta
- amelogenesis imperfecta, IIa 1K
- dentinogenesis imperfecta type 2
- dentinogenesis imperfecta type 3
- taurodontism
- amelogenesis imperfecta, type 3A
- otodental syndrome
- fused mandibular incisors
- Ackerman syndrome
