Disease #01560 (SPG4 (paraplegia, spastic, autosomal dominant, type 4 (SPG4)), OMIM:182601)
Official abbreviation |
SPG4 |
Name |
paraplegia, spastic, autosomal dominant, type 4 (SPG4) |
OMIM ID |
182601 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
12 |
Phenotype entries for this disease |
12 |
Associated with 1 gene |
SPAST |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-10-07 08:59:33 +02:00 (CEST) |
Individuals
|