Disease #02455 (CPSQ1 (palsy, cerebral, spastic quadriplegic, type 1 (CPSQ-1)), OMIM:603513)
Official abbreviation |
CPSQ1 |
Name |
palsy, cerebral, spastic quadriplegic, type 1 (CPSQ-1) |
OMIM ID |
603513 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
GAD1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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