Disease #03536 (SPG47;CPSQ5 (spastic paraplegia, type 47 (SPG-47, palsy, cerebral, spastic quadriplegic, type 5)), OMIM:614066)
| Official abbreviation |
SPG47;CPSQ5 |
| Name |
spastic paraplegia, type 47 (SPG-47, palsy, cerebral, spastic quadriplegic, type 5) |
| OMIM ID |
614066 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
AP4B1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|