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Alveolar rhabdomyosarcoma
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Ocular albinism with congenital sensorineural deafness
1 OMIM reference -
2 associated genes
No signs/symptoms info
Alveolar rhabdomyosarcoma
Ocular albinism with congenital sensorineural deafness

FOXO1
(UniProt - OMIM)
 MITF
(UniProt - OMIM)
PAX3
(UniProt - OMIM)
 TYR
(UniProt - OMIM)
PAX7
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PAX3
(0.52)
MITF


Citations in the biomedical literature:


Alveolar rhabdomyosarcoma
FOXO1 PAX3 PAX7
Ocular albinism with congenital sensorineural deafness
MITF TYR



Alveolar rhabdomyosarcoma
Ocular albinism with congenital sensorineural deafness

Synonym(s):
(no synonyms)

Synonym(s):
- Waardenburg syndrome type 2 with ocular albinism
Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D018232
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.