1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111003 | Joubert syndrome 8 | A Joubert syndrome that has_material_basis_in mutation in the ARL13B gene on chromosome 3q11.1-q11.2. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |