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Ocular albinism with congenital sensorineural deafness
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Ocular albinism with congenital sensorineural deafness
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MITF
(0.56)
APP


Citations in the biomedical literature:


Ocular albinism with congenital sensorineural deafness
MITF TYR
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Ocular albinism with congenital sensorineural deafness
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Waardenburg syndrome type 2 with ocular albinism
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic 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.