SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 616282
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0001258) Spastic paraplegia 97 / 7739
2
 (HPO:0003487) Babinski sign 179 / 7739
3
 (HPO:0002355) Difficulty walking 61 / 7739
4
 (HPO:0001347) Hyperreflexia 363 / 7739
5
 (HPO:0001760) Abnormality of the foot rare [HPO:skoehler] 96 / 7739
6
 (HPO:0003701) Proximal muscle weakness 105 / 7739
7
 (HPO:0003202) Skeletal muscle atrophy 281 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: