Meckel syndrome 5 (Q50349684)
Jump to navigation
Jump to search
A Meckel syndrome that has material basis in an autosomal recessive mutation of RPGRIP1L on chromosome 16q12.2.
- MKS5
- Meckel-Gruber syndrome, type 5
- MECKEL SYNDROME, TYPE 5; MKS5
- MECKEL SYNDROME, TYPE 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome 5 |
A Meckel syndrome that has material basis in an autosomal recessive mutation of RPGRIP1L on chromosome 16q12.2. |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference
1 reference