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MITF-related melanoma and renal cell carcinoma predisposition syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Ocular albinism with congenital sensorineural deafness
1 OMIM reference -
2 associated genes
No signs/symptoms info
MITF-related melanoma and renal cell carcinoma predisposition syndrome
Ocular albinism with congenital sensorineural deafness

MITF
(UniProt - OMIM)
 MITF
(UniProt - OMIM)
TYR
(UniProt - OMIM)

COMMON
GENES 		MITF


Citations in the biomedical literature:


MITF-related melanoma and renal cell carcinoma predisposition syndrome
MITF
Ocular albinism with congenital sensorineural deafness
TYR



MITF-related melanoma and renal cell carcinoma predisposition syndrome
Ocular albinism with congenital sensorineural deafness

Synonym(s):
(no synonyms)

Synonym(s):
- Waardenburg syndrome type 2 with ocular albinism
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.