1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0070403 | hypomyelinating leukodystrophy 26 | A hypomyelinating leukodystrophy characterized by severe psychomotor delay, predominantly involving motor and expressive language development, cerebral and cerebellar atrophy, and corpus callosum hypoplasia that has_material_basis_in homozygous mutation in the SLC35B2 gene on chromosome 6p21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:1443 | cerebral degeneration | A brain disease that is characterized by loss of structure or function of neurons, including death of neurons and loss of brain tissue. |
