KERATITIS FUGAX HEREDITARIA

General Information (adopted from Orphanet):

Synonyms, Signs: KERATOENDOTHELIITIS FUGAX HEREDITARIA
Number of Symptoms 6
OrphanetNr:
OMIM Id: 148200
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

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

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0007759) Opacification of the corneal stroma 77 / 7739
2
(HPO:0000491) Keratitis 21 / 7739
3
(OMIM) No permanent corneal opacities 1 / 7739
4
(HPO:0003621) Juvenile onset 105 / 7739
5
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
6
(OMIM) Acute attacks of keratitis occurring 2 to 8 times a year 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Valle (1964) described keratitis fugax hereditaria as a new entity in 10 members of 4 generations. (Fugax means fleeting; fugitive and centrifugal are from the same Latin root, fugere, meaning to flee.) The disease begins between the ages ...