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MITF-related melanoma and renal cell carcinoma predisposition syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant keratitis
1 OMIM reference -
1 associated gene
No signs/symptoms info
MITF-related melanoma and renal cell carcinoma predisposition syndrome
Autosomal dominant keratitis

MITF
(UniProt - OMIM)
 PAX6
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MITF
(0.92)
PAX6


Citations in the biomedical literature:


MITF-related melanoma and renal cell carcinoma predisposition syndrome
MITF
Autosomal dominant keratitis
PAX6



MITF-related melanoma and renal cell carcinoma predisposition syndrome
Autosomal dominant keratitis

Synonym(s):
(no synonyms)

Synonym(s):
- Hereditary keratitis
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537022
No signs/symptoms info available.