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Moderate multiminicore disease with hand involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
King-Denborough syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Moderate multiminicore disease with hand involvement
King-Denborough syndrome

RYR1
(UniProt - OMIM)
 RYR1
(UniProt - OMIM)

COMMON
GENES 		RYR1


Citations in the biomedical literature:


Moderate multiminicore disease with hand involvement
RYR1
King-Denborough syndrome



Moderate multiminicore disease with hand involvement
King-Denborough syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Koussef-Nichols syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C536883
No signs/symptoms info available.