Disease #02646 (HGPPS1 (Gaze palsy, familial horizontal, with progressive scoliosis, type 1), OMIM:607313)
| Official abbreviation |
HGPPS1 |
| Name |
Gaze palsy, familial horizontal, with progressive scoliosis, type 1 |
| OMIM ID |
607313 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ROBO3 |
| 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
|