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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
APC-related attenuated familial adenomatous polyposis
Epidermolysis bullosa simplex with circinate migratory erythema

APC KRT5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
KRT5



Citations in the biomedical literature:


APC-related attenuated familial adenomatous polyposis
APC
Epidermolysis bullosa simplex with circinate migratory erythema
KRT5



APC-related attenuated familial adenomatous polyposis
Epidermolysis bullosa simplex with circinate migratory erythema

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli

Synonym(s):
- EBS-migr

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

Classification (ICD10):
- Neoplasms -
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
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Epidermolysis bullosa simplex with circinate migratory erythema

Very frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Cutaneous rash
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment



APC-related attenuated familial adenomatous polyposis

(no data available)