Meckel syndrome 3 (Q50349682)
Jump to navigation
Jump to search
A Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1.
- MKS3
- Meckel-Gruber syndrome, type 3
- MECKEL SYNDROME, TYPE 3; MKS3
- MECKEL SYNDROME, TYPE 3
- Meckel syndrome type 3
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome 3 |
A Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1. |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference