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White sponge nevus
1 OMIM reference -
2 associated genes
15 connected diseases
No signs/symptoms info
Disease Type of connection
Pseudohypoaldosteronism type 2E
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Young adult-onset Parkinsonism
Congenital analbuminemia
46,XY partial gonadal dysgenesis
APC-related attenuated familial adenomatous polyposis
Amyotrophic lateral sclerosis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Cabezas syndrome
Desmoid tumor
Familial adenomatous polyposis due to 5q22.2 microdeletion
Fanconi anemia
Gardner syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Turcot syndrome with polyposis
Synonym(s):
- Hereditary mucosal leukokeratosis
- White sponge nevus of Cannon
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KRT13 P13646148065
KRT4 P19013123940
No signs/symptoms info available.