Familial congenital palsy of trochlear nerve

General Information (adopted from Orphanet):

Synonyms, Signs: STRABISMUS FROM SUPERIOR OBLIQUE PALSY
SUPERIOR OBLIQUE OCULOMOTOR PALSY, FAMILIAL CONGENITAL
TROCHLEAR NERVE PALSY, FAMILIAL CONGENITAL
Number of Symptoms 2
OrphanetNr: 91498
OMIM Id: 136480
ICD-10: H49.1
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Congenital trochlear nerve palsy
 -Rare eye disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
 (HPO:0007011) Fourth cranial nerve palsy 1 / 7739
2
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: