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Congenital reticular ichthyosiform erythroderma
1 OMIM reference -
1 associated gene
34 connected diseases
No signs/symptoms info
Disease Type of connection
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Cowden syndrome
Proteus syndrome
Common variable immunodeficiency
Congenital analbuminemia
Fibronectin glomerulopathy
Spinocerebellar ataxia type 12
B-cell chronic lymphocytic leukemia
Cabezas syndrome
Congenital bilateral absence of vas deferens
Cystic fibrosis
Dedifferentiated liposarcoma
Estrogen resistance syndrome
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Juvenile myelomonocytic leukemia
Leber congenital amaurosis
Lethal arthrogryposis - anterior horn cell disease
Lethal congenital contracture syndrome type 1
Male infertility with normal virilization due to meiosis defect
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Pseudohypoaldosteronism type 2E
Richieri Costa-Pereira syndrome
Senior-Loken syndrome
Well-differentiated liposarcoma
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Epidermolytic palmoplantar keratoderma
Ichthyosis hystrix of Curth-Macklin
Keratosis palmoplantaris striata
Superficial epidermolytic ichthyosis
- Ichthyosis variegata
- Ichthyosis with confetti

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
KRT10 P13645148080
No signs/symptoms info available.