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Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Mitochondrial nonsyndromic sensorineural deafness
2 OMIM references -
6 associated genes
No signs/symptoms info
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Mitochondrial nonsyndromic sensorineural deafness

TRMU
(UniProt - OMIM)
 MT-CO1
(UniProt - OMIM)
MT-RNR1
(OMIM)
MT-TH
(OMIM)
MT-TS1
(OMIM)
TFB1M
(UniProt - OMIM)
TRMU
(UniProt - OMIM)

COMMON
GENES 		TRMU


Citations in the biomedical literature:


Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
TRMU
Mitochondrial nonsyndromic sensorineural deafness
MT-CO1 MT-RNR1 MT-TH MT-TS1 TFB1M



Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Mitochondrial nonsyndromic sensorineural deafness

Synonym(s):
- Acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins
Synonym(s):
- Isolated mitochondrial neurosensory deafness
- Isolated mitochondrial sensorineural deafness
- Mitochondrial nonsyndromic neurosensory deafness
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Diseases of the ear and mastoid process -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: mitochondrial inheritance
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.