Thyrotoxic periodic paralysis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Thyrotoxic hypokalemic periodic paralysis |
| Number of Symptoms | 8 |
| OrphanetNr: | 79102 |
| OMIM Id: |
188580
613239 614834 |
| ICD-10: |
G72.3 |
| UMLs: |
C0268446 |
| MeSH: |
|
| MedDRA: |
10043788 |
| Snomed: |
30967002 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Multifactorial Not applicable [Orphanet] |
| Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Periodic paralysis
-Rare genetic disease -Rare neurologic disease |
Symptom Information:
|
|
(HPO:0003768) | Periodic paralysis | 9 / 7739 | ||||
|
|
(HPO:0000853) | Goiter | 39 / 7739 | ||||
|
|
(HPO:0000836) | Hyperthyroidism | 25 / 7739 | ||||
|
|
(HPO:0001962) | Palpitations | 62 / 7739 | ||||
|
|
(HPO:0002900) | Hypokalemia | 45 / 7739 | ||||
|
|
(HPO:0003201) | Rhabdomyolysis | 27 / 7739 | ||||
|
|
(HPO:0001324) | Muscle weakness | 859 / 7739 | ||||
|
|
(HPO:0001425) | Heterogeneous | 132 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|