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Congenital muscular dystrophy with hyperlaxity
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Keratosis follicularis spinulosa decalvans
Pediatric systemic lupus erythematosus
Synonym(s):
- CMDH
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ITGA9 Q13797603963
No signs/symptoms info available.