Genetic keratinization disorder associated with ocular features

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 1
OrphanetNr: 98697
OMIM Id:
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Genodermatosis with ocular features
 -Rare eye disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
(HPO:0008064) Ichthyosis Very frequent [Orphanet] 108 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: