Cytoscape Web
Click node...


PROTEIN INTERACTIONS: 7
5 OMIM references -
8 associated genes
No signs/symptoms info
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Familial pancreatic carcinoma

MT-CO1 BRCA1
MT-ND4 BRCA2
MT-RNR1 CDKN2A
MT-TS1 KRAS
TRMU MANF
PALB2
SMAD4
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MT-RNR1
MT-TS1
MT-ND4
MT-RNR1
MT-RNR1
MT-TS1
MT-TS1
(0.65)
(0.65)
(0.63)
(0.63)
(0.63)
(0.63)
(0.63)
BRCA1
BRCA1
SMAD4
CDKN2A
TP53
CDKN2A
TP53



Citations in the biomedical literature:


Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
MT-CO1 MT-ND4 MT-RNR1 MT-TS1 TRMU
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Familial pancreatic carcinoma

Synonym(s):
- Mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure
- Mitochondrial isolated neurosensory hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure
- Mitochondrial isolated sensorineural hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial nonsyndromic neurosensory deafness with susceptibility to aminoglycoside exposure
- Mitochondrial nonsyndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure
- Mitochondrial nonsyndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure

Synonym(s):
- Familial pancreatic cancer

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: mitochondrial inheritance
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.