CEREBELLOPARENCHYMAL DISORDER V

General Information (adopted from Orphanet):

Synonyms, Signs: SPINODENTATE ATROPHY
DYSSYNERGIA CEREBELLARIS MYOCLONICA OF HUNT
CPD5
Number of Symptoms 6
OrphanetNr:
OMIM Id: 213400
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001336) Myoclonus 115 / 7739
2
(HPO:0001251) Ataxia 413 / 7739
3
(HPO:0001939) Abnormality of metabolism/homeostasis 328 / 7739
4
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
5
(OMIM) Superior cerebellar peduncle fiber loss 1 / 7739
6
(OMIM) Dentate neuron loss 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: