Skip to main content
Diseases

Hereditary Autosomal Dominant Spastic Paraplegia

hereditary autosomal dominant spastic paraplegia

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Hereditary Autosomal Dominant Spastic Paraplegia
Standard Disease Name
hereditary autosomal dominant spastic paraplegia
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
No data
HPO ID
No data

Description and Extensions

Description
No data
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
DYRK3
dual specificity tyrosine phosphorylation regulated kinase 3
dual specificity tyrosine phosphorylation regulated kinase 3
03
ITPR1
inositol 1,4,5-trisphosphate receptor type 1
inositol 1,4,5-trisphosphate receptor type 1
07
SPG7
SPG7 matrix AAA peptidase subunit, paraplegin
SPG7 matrix AAA peptidase subunit, paraplegin