Neurodevelopmental Disorder With Cerebellar Atrophy And Motor Dysfunction
Disease ID: disease_node_16435
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| Dbxref | MIM:619333 |
|---|---|
| Subclassof | DOID_0060308 |
| Data Source | DOID |
| Doid Label | neurodevelopmental disorder with cerebellar atrophy and motor dysfunction |
| Doid Description | An autosomal recessive intellectual developmental disorder characterized by cerebellar atrophy and global developmental delay with cognitive impairment, speech delay, and prominent motor abnormalities including axial hypotonia, gait ataxia, and appendicular spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the GEMIN5 gene on chromosome 5q33.2. |
| Disease Node Id | disease_node_16435 |
| Doid Id | DOID_0070443 |
| Label | Neurodevelopmental Disorder With Cerebellar Atrophy And Motor Dysfunction |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Intellectual Developmental Disorder(ID:disease_node_16368) (Disease)