EVX2
Description
The EVX2 (even-skipped homeobox 2) is a protein-coding gene located on chromosome 2.
EVX2 is also known as EVX-2.
Associated Diseases
- Parkinson disease
- multiple sclerosis
- Alzheimer disease
- lysosomal storage disease
- brachydactyly type A2
- familial digital arthropathy-brachydactyly
- brachydactyly type C
- brachydactyly-elbow wrist dysplasia syndrome
- thumb stiffness-brachydactyly-intellectual disability syndrome
- Thiemann disease, familial form
- brachydactyly-syndactyly syndrome
- brachydactyly type A1
- upper limb mesomelic dysplasia
- Leri-Weill dyschondrosteosis
- acromesomelic dysplasia 2C, Hunter-Thompson type
- syndactyly type 5
- ectrodactyly-polydactyly syndrome
- postaxial tetramelic oligodactyly
- brachydactyly-preaxial hallux varus syndrome
