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Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive limb-girdle muscular dystrophy type 2S
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Autosomal recessive limb-girdle muscular dystrophy type 2S

TRAPPC11
(UniProt - OMIM)
 TRAPPC11
(UniProt - OMIM)

COMMON
GENES 		TRAPPC11


Citations in the biomedical literature:


Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
TRAPPC11
Autosomal recessive limb-girdle muscular dystrophy type 2S



Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Autosomal recessive limb-girdle muscular dystrophy type 2S

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD2S
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.