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4 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Dowling-Degos disease
Turcot syndrome with polyposis

KRT5 APC
POFUT1
POGLUT1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Dowling-Degos disease
KRT5 POFUT1 POGLUT1
Turcot syndrome with polyposis
APC



Dowling-Degos disease
Turcot syndrome with polyposis

Synonym(s):
- Reticular pigment anomaly of flexures

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.