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Familial congenital palsy of trochlear nerve
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Inherited congenital spastic tetraplegia
2 OMIM references -
3 associated genes
No signs/symptoms info
Familial congenital palsy of trochlear nerve
Inherited congenital spastic tetraplegia

KANK1
(UniProt - OMIM)
 ADD3
(UniProt - OMIM)
GAD1
(UniProt - OMIM)
KANK1
(UniProt - OMIM)

COMMON
GENES 		KANK1


Citations in the biomedical literature:


Familial congenital palsy of trochlear nerve
KANK1
Inherited congenital spastic tetraplegia
ADD3 GAD1



Familial congenital palsy of trochlear nerve
Inherited congenital spastic tetraplegia

Synonym(s):
(no synonyms)

Synonym(s):
- Inherited congenital spastic quadriplegia
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.