| Disease ID | Source | Name | Description |
| 614728 | OMIM | Seckel syndrome 6 (SCKL6) | A rare autosomal recessive disorder characterized by proportionate dwarfism of prenatal onset associated with low birth weight, growth retardation, severe microcephaly with a bird-headed like appearance, and mental retardation. The disease is caused by variants affecting the gene represented in this entry. |