Disease #00213 (SPG10 (paraplegia, spastic, autosomal dominant, type 10 (SPG-10)), OMIM:604187)
Official abbreviation |
SPG10 |
Name |
paraplegia, spastic, autosomal dominant, type 10 (SPG-10) |
OMIM ID |
604187 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
KIF5A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-10-02 11:35:03 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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