| Metadata | |
|---|---|
| ID | DOID:0070120 |
| Name | Meckel syndrome 6 |
| Definition | A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32. https://www.ncbi.nlm.nih.gov/pubmed/18513680 |
| Xrefs | |
| Synonyms |
Meckel-Gruber syndrome, type 6 [EXACT] MKS6 [EXACT] |
| Parent Relationships |
is_a Meckel syndrome |