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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
6 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Mitochondrial nonsyndromic sensorineural deafness

HSPD1 MT-CO1
MT-RNR1
MT-TH
MT-TS1
TFB1M
TRMU


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.55)
MT-CO1



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Mitochondrial nonsyndromic sensorineural deafness
MT-CO1 MT-RNR1 MT-TH MT-TS1 TFB1M TRMU



Autosomal dominant spastic paraplegia type 13
Mitochondrial nonsyndromic sensorineural deafness

Synonym(s):
- SPG13

Synonym(s):
- Isolated mitochondrial neurosensory deafness
- Isolated mitochondrial sensorineural deafness
- Mitochondrial nonsyndromic neurosensory deafness

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the ear and mastoid process -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: mitochondrial inheritance

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.