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Moderate multiminicore disease with hand involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Thyrotoxic periodic paralysis
3 OMIM references -
3 associated genes
No signs/symptoms info
Moderate multiminicore disease with hand involvement
Thyrotoxic periodic paralysis

RYR1
(UniProt - OMIM)
 CACNA1S
(UniProt - OMIM)
GABRA3
(UniProt - OMIM)
KCNJ18
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RYR1
(0.62)
CACNA1S


Citations in the biomedical literature:


Moderate multiminicore disease with hand involvement
RYR1
Thyrotoxic periodic paralysis
CACNA1S GABRA3 KCNJ18



Moderate multiminicore disease with hand involvement
Thyrotoxic periodic paralysis

Synonym(s):
(no synonyms)

Synonym(s):
- Thyrotoxic hypokalemic periodic paralysis
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.