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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 3
48 OMIM references -
31 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Autosomal dominant nonsyndromic sensorineural deafness type DFNA

APP ACTG1
CCDC50
CEACAM16
COCH
COL11A2
CRYM
DFNA5
DIABLO
DIAPH1
DIAPH3
EYA4
GJB2
GJB3
GJB6
GRHL2
KCNQ4
MIR96
MYH14
MYH9
MYO1A
MYO6
MYO7A
P2RX2
POU4F3
SIX1
SLC17A8
TECTA
TJP2
TMC1
TNC
WFS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
APP
APP
(0.63)
(0.56)
(0.56)
MYH9
GRHL2
MIR96



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
ACTG1 CCDC50 CEACAM16 COCH COL11A2 CRYM
DFNA5 DIABLO DIAPH1 DIAPH3 EYA4 GJB2
GJB3 GJB6 GRHL2 KCNQ4 MIR96 MYH14
MYH9 MYO1A MYO6 MYO7A P2RX2 POU4F3
SIX1 SLC17A8 TECTA TJP2 TMC1 TNC
WFS1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Autosomal dominant nonsyndromic sensorineural deafness type DFNA

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Autosomal dominant isolated neurosensory deafness type DFNA
- Autosomal dominant isolated neurosensory hearing loss type DFNA
- Autosomal dominant isolated sensorineural deafness type DFNA
- Autosomal dominant isolated sensorineural hearing loss type DFNA
- Autosomal dominant nonsyndromic neurosensory deafness type DFNA
- Autosomal dominant nonsyndromic neurosensory hearing loss type DFNA
- Autosomal dominant nonsyndromic sensorineural hearing loss type DFNA

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the ear and mastoid process -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.